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50-69-1

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  • D-Ribose / intermediate/white powder with CAS NO.50-69-1/ worldwide Top Pharma factory vendor with most competitive price

    Cas No: 50-69-1

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50-69-1 Usage

Description

D-ribose is an important five-carbon monosaccharide with the chemical formula C5H10O5. It is an important constituent of ribonucleic acid (RNA) and ATP, and plays an important role in the formation of life. It is also an important pharmaceutical intermediate for the production of various nucleic acid drugs.

Chemical Properties

D-Ribose is a five-carbon sugar with strong water solubility and sweet taste, also known as D-ribofuranose. It is used by all living cells and is an essential component in living organisms for energy production. It is widely present in the furan form.

Occurrence

Reported found in boiled crab, hen egg, catfish, whitefish, haddock, stored beef, stored veal, milk, applesauce, potato, rapeseed, roasted coffee, fresh coffee and shrimp.

Uses

D-Ribose is produced by microorganism fermentation of glucose in a fermentation culture medium without adding calcium carbonate.

Preparation

D-Ribose is obtained by using D-glucose as a raw material, inserting bacteria or Bacillus subtilis for fermentation, and separating and refining the fermentation product.(By fermentation technology)

Definition

ChEBI: D-ribose is a ribofuranose having D-configuration. It is a naturally occurring monosaccharide found in the cells and particularly in the mitochondria is essential in energy production.

Biological Activity

D-ribose is a natural sugar that our bodies produce for a variety of purposes most notably encrgy in the form of ATP(adenosine triphosphate), which powers every cell in our body. Ribose is crucial for the synthesis of energy (ATP) and without it, your cells run out of energy and the health of the cell is compromised. Supplementing with ribose improves cell function by restoring energy. One of the most vital organs to suffer energy depletion is the heart. That is why so much of the research on D-ribose has focused on the impact of supplement ribose in heart disease. Although ribose is classified as a sugar, when taken orally, it does not have any impact on blood sugar like glucose. Instead, it is used for energy production and energy recovery. Every cell in the body has the capacity to make ribose. But more ribose may be needed than the cell can produce when cells are metabolically stressed, such as with strenuous exercise or disease. When the cells are metabolically stressed they tend to consume more glucose rather than producing more ribose. This can dramatically affect recovery.

Biochem/physiol Actions

Ribose is an aldopentose monosaccharide that is phosphorylated into D-ribose 5-phosphate by ribokinase.

Side effects

D-ribose is a dietary supplement approved by the US FDA. It is generally considered safe for dosage of ribose is less than 15g/d. However, possible side effects include diarrhea, stomach discomfort, nausea, headache, and low blood sugar.

Purification Methods

Crystallise -D(-)-ribose from aqueous 80% EtOH, dry it under vacuum at 60o over P2O5 and store it in a vacuum desiccator. It exhibits a complex mutarotation with : [] D 10 -23.1o (1.5minutes), -21.3o (5minutes), -19.5o (10minutes), -19.1o (30minutes), -21.2o (60minutes), -23.1o (120minutes), -23.7o (300minutes), (c 4.5, H2O) [Phelps et al. J Am Chem Soc 56 748 1934]. 1H NMR in D2O at 44o shows 17% -pyranose, 59% -pyranose, 9% -furanose and 15% -furanose forms with furanose -H at 5.34ppm (J 3.0Hz) and -H at 5.31 (J 1.7Hz) [Angyal Adv Carbohydr Chem 42 15 1984, Angyal & Pickles Aust J Chem 25 1711 1972]. The phenylhydrazone crystallises from aqueous pyridine in yellow needles, m 163-164o, and the benzylphenylhydrazone has m 127-128o [Snowden J Am Chem Soc 72 808 1950.] [Beilstein 1 IV 4211.]

Check Digit Verification of cas no

The CAS Registry Mumber 50-69-1 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50-69:
(4*5)+(3*0)+(2*6)+(1*9)=41
41 % 10 = 1
So 50-69-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O5/c6-1-2-3(7)4(8)5(9)10-2/h2-9H,1H2/t2-,3-,4-,5-/m1/s1

50-69-1 Well-known Company Product Price

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  • TCI America

  • (R0025)  D-(-)-Ribose  >98.0%(GC)

  • 50-69-1

  • 25g

  • 390.00CNY

  • Detail
  • TCI America

  • (R0025)  D-(-)-Ribose  >98.0%(GC)

  • 50-69-1

  • 250g

  • 2,350.00CNY

  • Detail
  • Alfa Aesar

  • (A17894)  D-(-)-Ribose, 98%   

  • 50-69-1

  • 10g

  • 124.0CNY

  • Detail
  • Alfa Aesar

  • (A17894)  D-(-)-Ribose, 98%   

  • 50-69-1

  • 50g

  • 473.0CNY

  • Detail
  • Alfa Aesar

  • (A17894)  D-(-)-Ribose, 98%   

  • 50-69-1

  • 250g

  • 2188.0CNY

  • Detail
  • USP

  • (1603108)  Ribose  United States Pharmacopeia (USP) Reference Standard

  • 50-69-1

  • 1603108-300MG

  • 4,588.74CNY

  • Detail

50-69-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name aldehydo-D-ribose

1.2 Other means of identification

Product number -
Other names D-RIB

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:50-69-1 SDS

50-69-1Synthetic route

1,5-Anhydro-2,3-O-isopropylidene-β-D-ribofuranose
51246-99-2

1,5-Anhydro-2,3-O-isopropylidene-β-D-ribofuranose

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With trifluoroacetic acid at 20℃;90%
Conditions
ConditionsYield
With K 10 clay In methanol; water at 50℃; for 72h;75%
D-Arabinose
10323-20-3

D-Arabinose

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With molybdic acid In water for 0.05h; Bilik reaction; microwave irradiation;30%
With borax In water at 69.84℃; for 1h; Kinetics; pH-value; stereospecific reaction;
With HNbMoO6 In water at 119.84℃; for 3h; Reagent/catalyst;
With caesium modified hydrated phosphomolybdic acid supported on activated carbon In water at 59.84℃; for 0.5h; Catalytic behavior;
pyridine
110-86-1

pyridine

D-ribulose
488-84-6

D-ribulose

A

D-Arabinose
10323-20-3

D-Arabinose

B

D-ribose
50-69-1

D-ribose

pyridine
110-86-1

pyridine

xylulose
551-84-8

xylulose

A

D-xylose
58-86-6

D-xylose

B

D-Arabinose
10323-20-3

D-Arabinose

C

D-ribose
50-69-1

D-ribose

nitromethane
75-52-5

nitromethane

sodium methylate
124-41-4

sodium methylate

D-erythrose
583-50-6

D-erythrose

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With methanol Eintragen einer wss.Loesung des Reaktionsprodukts in wss.Schwefelsaeure bei -20grad;
O2-methanesulfonyl-D-arabinose
67006-18-2

O2-methanesulfonyl-D-arabinose

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With barium dihydroxide; water
D-ribonic acid
642-98-8

D-ribonic acid

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With sodium amalgam
2,3,4,5-tetra-O-acetyl-aldehydo-D-ribose
30571-54-1

2,3,4,5-tetra-O-acetyl-aldehydo-D-ribose

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With barium dihydroxide; water
D-glycero-D-manno-[2]octulose
13111-79-0

D-glycero-D-manno-[2]octulose

lead(IV) tetraacetate
546-67-8

lead(IV) tetraacetate

acetic acid
64-19-7

acetic acid

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
und Erwaermen des Reaktionsprodukts mit Wasser;
Perbenzoic acid
93-59-4

Perbenzoic acid

chloroform
67-66-3

chloroform

1,5-anhydro-2-deoxy-D-erythro-pent-1-enitol
496-61-7

1,5-anhydro-2-deoxy-D-erythro-pent-1-enitol

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
at 0℃;
D-Ribono-1,4-lactone
5336-08-3

D-Ribono-1,4-lactone

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With sulfuric acid; sodium sulfate Reduktion an einer Quecksilber-Kathode;
With sodium amalgam; sulfuric acid; water
With sodium amalgam; sodium hydrogen oxalate
D-erythro-pentos-2-ulose
3445-24-7

D-erythro-pentos-2-ulose

A

D-Arabitol
488-82-4

D-Arabitol

B

Adonitol
488-81-3

Adonitol

C

D-ribulose
488-84-6

D-ribulose

D

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With hydrogen; palladium on activated charcoal In water at 80℃; for 0.5h;A n/a
B n/a
C 70 % Chromat.
D n/a
oleanolic acid 3-O-β-D-ribopyranosyl-(1-3)-α-L-rhamnopyranosyl-(1-2)-α-L-arabinopyranoside
75799-17-6, 75799-18-7, 96315-51-4, 104494-26-0, 142628-40-8

oleanolic acid 3-O-β-D-ribopyranosyl-(1-3)-α-L-rhamnopyranosyl-(1-2)-α-L-arabinopyranoside

A

L-rhamnose
6014-42-2

L-rhamnose

B

L-arabinose
7296-55-1

L-arabinose

C

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With hydrogenchloride In methanol for 2h; Heating;A n/a
B n/a
C n/a
D 3 mg
(2R,3S,4S)-5-[(Z)-5-Amino-6-methyl-pyrimidin-4-ylimino]-pentane-1,2,3,4-tetraol

(2R,3S,4S)-5-[(Z)-5-Amino-6-methyl-pyrimidin-4-ylimino]-pentane-1,2,3,4-tetraol

A

4,5-diamino-6-methylpyrimidine
22715-28-2

4,5-diamino-6-methylpyrimidine

B

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With sodium hydroxide at 90.1℃; Mechanism; Rate constant; hydroxide ion concentration influence;
(2R,3S,4S)-5-[(Z)-5-Amino-6-chloro-pyrimidin-4-ylimino]-pentane-1,2,3,4-tetraol

(2R,3S,4S)-5-[(Z)-5-Amino-6-chloro-pyrimidin-4-ylimino]-pentane-1,2,3,4-tetraol

A

6-chloro-4,5-diaminopyrimidine
4316-98-7

6-chloro-4,5-diaminopyrimidine

B

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With sodium hydroxide at 50.1℃; Mechanism; Rate constant; hydroxide concentration influence;
(2R,3S,4S)-5-[(Z)-5-Amino-6-methylsulfanyl-pyrimidin-4-ylimino]-pentane-1,2,3,4-tetraol

(2R,3S,4S)-5-[(Z)-5-Amino-6-methylsulfanyl-pyrimidin-4-ylimino]-pentane-1,2,3,4-tetraol

A

4,5-diamino-6-methylthiopyrimidine
6965-92-0

4,5-diamino-6-methylthiopyrimidine

B

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With sodium hydroxide at 90.1℃; Mechanism; hydroxide ion concentration influence;
6-methyluridine
16710-13-7

6-methyluridine

A

6-Methyluracil
626-48-2

6-Methyluracil

B

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With sodium hydroxide at 90.1℃; Rate constant; Mechanism; various reagent concentration, decomposition to nonchromophoric products;
6-methyl-cytidine
16710-12-6

6-methyl-cytidine

A

6-Methyluracil
626-48-2

6-Methyluracil

B

6-Methyl-2(1H)-pyrimidinone
6220-50-4

6-Methyl-2(1H)-pyrimidinone

C

D-ribose
50-69-1

D-ribose

D

6-methyluridine
16710-13-7

6-methyluridine

Conditions
ConditionsYield
With sodium hydroxide at 90.1℃; Rate constant; Mechanism; various reagent concentration, decomposition to nonchromophoric products;
D-Ribono-1,4-lactone
5336-08-3

D-Ribono-1,4-lactone

mercury-cathode

mercury-cathode

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
elektrochemische Reduktion;
D-Ribono-1,4-lactone
5336-08-3

D-Ribono-1,4-lactone

sodium-amalgam

sodium-amalgam

diluted aqueous sulfuric acid

diluted aqueous sulfuric acid

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
bei verschiedenem pH;
(3R)-3,4-dihydro-2H-pyran-3r,4c-diol

(3R)-3,4-dihydro-2H-pyran-3r,4c-diol

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With Perbenzoic acid; water; ethyl acetate
O4-formyl-O2-methanesulfonyl-D-arabinose
116009-82-6

O4-formyl-O2-methanesulfonyl-D-arabinose

aqueous NaOH-solution

aqueous NaOH-solution

D-ribose
50-69-1

D-ribose

1-Deoxy-1-nitro-D-ribitol
130930-30-2

1-Deoxy-1-nitro-D-ribitol

aqueous NaOH-solution

aqueous NaOH-solution

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
anschliessendes Behandeln mit wss.Schwefelsaeure;
O2-methanesulfonyl-D-arabinose
67006-18-2

O2-methanesulfonyl-D-arabinose

water
7732-18-5

water

barium hydroxide

barium hydroxide

D-ribose
50-69-1

D-ribose

calcium salt of/the/ D-altronic acid

calcium salt of/the/ D-altronic acid

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With water; barium(II) acetate; iron(II) sulfate Erwaermen der reaktionsloesung mit wss.Wasserstoffperoxid;
copper (I)-salt of/the/ adenylic acid

copper (I)-salt of/the/ adenylic acid

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With sulfuric acid
copper (I)-salt of/the/ guanylic acid

copper (I)-salt of/the/ guanylic acid

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With sulfuric acid
dihydrouridine

dihydrouridine

D-ribose
50-69-1

D-ribose

Conditions
ConditionsYield
With sulfuric acid
D-ribose
50-69-1

D-ribose

methylamine
74-89-5

methylamine

N-methylribitylamine
7115-47-1

N-methylribitylamine

Conditions
ConditionsYield
Stage #1: D-ribose; methylamine In methanol at 20℃; for 4h;
Stage #2: With hydrogen; platinum(IV) oxide In methanol under 2068.59 Torr; for 12h;
100%
With hydrogen; nickel
D-ribose
50-69-1

D-ribose

phenylboronic acid
98-80-6

phenylboronic acid

C11H13BO5

C11H13BO5

Conditions
ConditionsYield
In methanol; water at 20℃; for 2h;100%
D-ribose
50-69-1

D-ribose

benzylamine
100-46-9

benzylamine

C12H17NO4
1361940-14-8

C12H17NO4

Conditions
ConditionsYield
In methanol at 20 - 45℃; for 3h;100%
D-ribose
50-69-1

D-ribose

ethanethiol
75-08-1

ethanethiol

D-ribose diethyl dithioacetal
7152-47-8

D-ribose diethyl dithioacetal

Conditions
ConditionsYield
With hydrogenchloride In water at 0℃; for 2h; Inert atmosphere;99%
With hydrogenchloride at 0℃; for 0.5h; Condensation;75%
With dimethylbromosulphonium bromide at 0 - 5℃; for 0.5h; neat (no solvent);72%
D-ribose
50-69-1

D-ribose

Trimethylenediamine
109-76-2

Trimethylenediamine

hexahydro-2-(D-ribo-1,2,3,4-tetrahydroxybutyl)pyrimidine

hexahydro-2-(D-ribo-1,2,3,4-tetrahydroxybutyl)pyrimidine

Conditions
ConditionsYield
for 34h; Cyclization;99%
D-ribose
50-69-1

D-ribose

1,1-dimethylhydrazine
57-14-7

1,1-dimethylhydrazine

(2S,3R,4S,E)-5-(2,2-dimethylhydrazono)pentane-1,2,3,4-tetraol

(2S,3R,4S,E)-5-(2,2-dimethylhydrazono)pentane-1,2,3,4-tetraol

Conditions
ConditionsYield
With Amberlyst 15 In methanol at 20℃; for 24h;98%
carbonic acid bis(1-isopropylhydrazide) dihydrochloride

carbonic acid bis(1-isopropylhydrazide) dihydrochloride

D-ribose
50-69-1

D-ribose

1'S,2'S,3'R-2,4-diisopropyl-6-(1',2',3',4'-tetrahydroxybutyl)-1,2,4,5-tetrazinan-3-one

1'S,2'S,3'R-2,4-diisopropyl-6-(1',2',3',4'-tetrahydroxybutyl)-1,2,4,5-tetrazinan-3-one

Conditions
ConditionsYield
With sodium acetate In water at 20℃;98%
D-ribose
50-69-1

D-ribose

2,3-Diaminonaphthalene
771-97-1

2,3-Diaminonaphthalene

(1'S,2'S,3'R,)-2-[1',2',3',4'-tetrahydroxybutyl]-1H-naphthimidazole
1027103-27-0

(1'S,2'S,3'R,)-2-[1',2',3',4'-tetrahydroxybutyl]-1H-naphthimidazole

Conditions
ConditionsYield
With air; iodine; acetic acid at 20℃; for 3h;97%
Conditions
ConditionsYield
With sulfuric acid at 20℃; for 4h;96%
With sulfuric acid at 20℃; for 2.5h;93%
With sulfuric acid Reagent/catalyst;93%
2-hydrazinoquinoline
15793-77-8

2-hydrazinoquinoline

D-ribose
50-69-1

D-ribose

(2R,3S,4S)-5-(Quinolin-2-yl-hydrazono)-pentane-1,2,3,4-tetraol

(2R,3S,4S)-5-(Quinolin-2-yl-hydrazono)-pentane-1,2,3,4-tetraol

Conditions
ConditionsYield
With acetic acid In ethanol for 1.5h; Heating;96%
D-ribose
50-69-1

D-ribose

acetone
67-64-1

acetone

2,3-O-Isopropylidene-D-ribose
13199-25-2

2,3-O-Isopropylidene-D-ribose

Conditions
ConditionsYield
With sulfuric acid96%
With sulfuric acid at 20℃;93%
With sulfuric acid at 20℃; for 24h; Inert atmosphere;90%
D-ribose
50-69-1

D-ribose

acetylacetone
123-54-6

acetylacetone

4,8-anhydro-1,3-dideoxy-β-D-glycero-D-allo-octulose

4,8-anhydro-1,3-dideoxy-β-D-glycero-D-allo-octulose

Conditions
ConditionsYield
With sodium carbonate In water at 90℃; for 1h; stereoselective reaction;96%
L-Cysteine
52-90-4

L-Cysteine

D-ribose
50-69-1

D-ribose

2(R,S)-D-ribo-(1',2',3',4'-tetrahydroxybutyl)-thiazolidine-4(R)-carboxylic acid
232617-15-1

2(R,S)-D-ribo-(1',2',3',4'-tetrahydroxybutyl)-thiazolidine-4(R)-carboxylic acid

Conditions
ConditionsYield
In ethanol; water at 18 - 20℃; for 26h; Inert atmosphere; Industry scale;95.65%
With potassium acetate
D-ribose
50-69-1

D-ribose

allyl bromide
106-95-6

allyl bromide

(2R,3R,4S)-1,2,3,4,5-pentahydroxyoct-7-ene
195196-45-3

(2R,3R,4S)-1,2,3,4,5-pentahydroxyoct-7-ene

Conditions
ConditionsYield
With indium In water for 10h; Barbier reaction;95%
With tin In ethanol for 16h; Heating;
With indium(III) chloride; tin 1.) H2O, 23 deg C, 4 h, 2.) H2O, 23 deg C, 24 h; Multistep reaction;
methanol
67-56-1

methanol

D-ribose
50-69-1

D-ribose

2,2-dimethoxy-propane
77-76-9

2,2-dimethoxy-propane

((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol
4099-85-8

((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol

Conditions
ConditionsYield
With hydrogenchloride In acetone at 20℃;95%
With hydrogenchloride In acetone at 0 - 20℃;75%
With hydrogenchloride In acetone at 20℃; for 20h;74%
D-ribose
50-69-1

D-ribose

4,5-dimethyl-1,2-phenylenediamine
3171-45-7

4,5-dimethyl-1,2-phenylenediamine

5,6-dimethylbenzimidazole-2-d

5,6-dimethylbenzimidazole-2-d

Conditions
ConditionsYield
With air In water-d295%
methanol
67-56-1

methanol

D-ribose
50-69-1

D-ribose

acetone
67-64-1

acetone

((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol
4099-85-8

((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol

Conditions
ConditionsYield
With sulfuric acid at 20℃; Inert atmosphere;95%
With hydrogenchloride In water for 18h; Heating / reflux;
Conditions
ConditionsYield
With sulfuric acid at 0 - 20℃; for 6h; Inert atmosphere;95%
With hydrogenchloride In methanol; water at 20 - 60℃;
D-ribose
50-69-1

D-ribose

ammonium carbamate
1111-78-0

ammonium carbamate

(2R,3R,4R,5R)-2-Amino-tetrahydro-pyran-3,4,5-triol; compound with carbamic acid

(2R,3R,4R,5R)-2-Amino-tetrahydro-pyran-3,4,5-triol; compound with carbamic acid

Conditions
ConditionsYield
With ammonium hydroxide In methanol at 37℃; for 3h;94%
D-ribose
50-69-1

D-ribose

(2-amino-4,5-dimethyl-phenyl)-carbamic acid tert-butyl ester
371158-46-2

(2-amino-4,5-dimethyl-phenyl)-carbamic acid tert-butyl ester

N-(ribityl),N'-(Boc)-diamino-4,5-dimethylbenzene
569343-11-9

N-(ribityl),N'-(Boc)-diamino-4,5-dimethylbenzene

Conditions
ConditionsYield
With sodium cyanoborohydride In methanol for 48h; Inert atmosphere; Reflux;94%
With sodium cyanoborohydride In methanol at 65℃; for 48h;92%
With sodium cyanoborohydride In methanol for 64h; Reflux;86%
With hydrogen; palladium dihydroxide In methanol for 2h;85 mg
With sodium cyanoborohydride In methanol at 65℃; for 48h;
methanol
67-56-1

methanol

D-ribose
50-69-1

D-ribose

2,2-dimethoxy-propane
77-76-9

2,2-dimethoxy-propane

acetone
67-64-1

acetone

Conditions
ConditionsYield
With hydrogenchloride at 20℃; for 48h;94%
L-Cysteine
52-90-4

L-Cysteine

D-ribose
50-69-1

D-ribose

C8H14NO6S(1-)*Na(1+)

C8H14NO6S(1-)*Na(1+)

Conditions
ConditionsYield
With sodium hydroxide at 80℃; pH=9.5; Temperature; Flow reactor;94%
D-ribose
50-69-1

D-ribose

4-amino-o-xylene
95-64-7

4-amino-o-xylene

3,4-dimethyl-N-ribitylaniline
3051-94-3

3,4-dimethyl-N-ribitylaniline

Conditions
ConditionsYield
With sodium cyanoborohydride In methanol for 72h; Reflux;93%
With sodium cyanoborohydride In methanol at 65℃; Inert atmosphere;92%
With sodium cyanoborohydride In methanol at 65℃; for 48h;90%
D-ribose
50-69-1

D-ribose

4-Chloro-1,2-phenylenediamine
95-83-0

4-Chloro-1,2-phenylenediamine

(1S,2S,3R)-2-(1,2,3,4-tetrahydroxybutyl)-1H-6-chlorobenzimidazole
1609208-16-3

(1S,2S,3R)-2-(1,2,3,4-tetrahydroxybutyl)-1H-6-chlorobenzimidazole

Conditions
ConditionsYield
With iodine In water; acetic acid at 20℃; for 3h;93%
D-ribose
50-69-1

D-ribose

acetone
67-64-1

acetone

(3aR,6aR)-6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol

(3aR,6aR)-6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-ol

Conditions
ConditionsYield
With sulfuric acid93%
D-ribose
50-69-1

D-ribose

acetic acid
64-19-7

acetic acid

(3R,4R,5R)-tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate
4627-30-9

(3R,4R,5R)-tetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate

Conditions
ConditionsYield
With pyridine; dmap Inert atmosphere;93%
D-ribose
50-69-1

D-ribose

Octanethiol
111-88-6

Octanethiol

D-Ribose-S,S-dioctylacetal

D-Ribose-S,S-dioctylacetal

Conditions
ConditionsYield
With hydrogenchloride at 40℃; for 1h;91.93%
D-ribose
50-69-1

D-ribose

methylhydrazine
60-34-4

methylhydrazine

(2R,3S,4S)-5-(Methyl-hydrazono)-pentane-1,2,3,4-tetraol
95405-73-5

(2R,3S,4S)-5-(Methyl-hydrazono)-pentane-1,2,3,4-tetraol

Conditions
ConditionsYield
In methanol for 1h; Ambient temperature;91%

50-69-1Relevant articles and documents

Thermal Behavior of d-Ribose Adsorbed on Silica: Effect of Inorganic Salt Coadsorption and Significance for Prebiotic Chemistry

Akouche, Mariame,Jaber, Maguy,Zins, Emilie-Laure,Maurel, Marie-Christine,Lambert, Jean-Francois,Georgelin, Thomas

, p. 15834 - 15846 (2016)

Understanding ribose reactivity is a crucial step in the “RNA world” scenario because this molecule is a component of all extant nucleotides that make up RNA. In solution, ribose is unstable and susceptible to thermal destruction. We examined how ribose behaves upon thermal activation when adsorbed on silica, either alone or with the coadsorption of inorganic salts (MgCl2, CaCl2, SrCl2, CuCl2, FeCl2, FeCl3, ZnCl2). A combination of13C NMR, in situ IR, and TGA analyses revealed a variety of phenomena. When adsorbed alone, ribose remains stable up to 150 °C, at which point ring opening is observed, together with minor oxidation to a lactone. All the metal salts studied showed specific interactions with ribose after dehydration, resulting in the formation of polydentate metal ion complexes. Anomeric equilibria were affected, generally favoring ribofuranoses. Zn2+stabilized ribose up to higher temperatures than bare silica (180 to 200 °C). Most other cations had an adverse effect on ribose stability, with ring opening already upon drying at 70 °C. In addition, alkaline earth cations catalyzed the dehydration of ribose to furfural and, to variable degrees, its further decarbonylation to furan. Transition-metal ions with open d-shells took part in redox reactions with ribose, either as reagents or as catalysts. These results allow the likelihood of prebiotic chemistry scenarios to be evaluated, and may also be of interest for the valorization of biomass-derived carbohydrates by heterogeneous catalysis.

Comprehensive investigation of the energetics of pyrimidine nucleoside formation in a model prebiotic reaction

Sheng, Yinghong,Bean, Heather D.,Mamajanov, Irena,Hud, Nicholas V.,Leszczynski, Jerzy

, p. 16088 - 16095 (2009)

The problem of β-nucleoside formation under prebiotic conditions represents one of the most significant challenges to the "RNA world" hypothesis. The possibility exists that alternative bases may have come before the contemporary bases (i.e., A, G, C, and

Biosynthesis of anti-HCV compounds using thermophilic microorganisms

Rivero, Cintia W.,De Benedetti, Eliana C.,Sambeth, Jorge E.,Lozano, Mario E.,Trelles, Jorge A.

, p. 6059 - 6062 (2012)

This work describes the application of thermophilic microorganisms for obtaining 6-halogenated purine nucleosides. Biosynthesis of 6-chloropurine- 2′-deoxyriboside and 6-chloropurine riboside was achieved by Geobacillus stearothermophilus CECT 43 with a conversion of 90% and 68%, respectively. Furthermore, the selected microorganism was satisfactorily stabilized by immobilization in an agarose matrix. This biocatalyst can be reused at least 70 times without significant loss of activity, obtaining 379 mg/L of 6-chloropurine-2′-deoxyriboside. The obtained compounds can be used as antiviral agents.

-

Sato

, (1951)

-

-

Steiger

, p. 189,191 (1936)

-

Biochemical characterization of a recombinant acid phosphatase from Acinetobacter baumannii

Smiley-Moreno, Elizabeth,Smith, Douglas,Yu, Jieh-Juen,Cao, Phuong,Arulanandam, Bernard P.,Chambers, James P.

, (2021/06/09)

Genomic sequence analysis of Acinetobacter baumannii revealed the presence of a putative Acid Phosphatase (AcpA; EC 3.1.3.2). A plasmid construct was made, and recombinant protein (rAcpA) was expressed in E. coli. PAGE analysis (carried out under denaturing/ reducing conditions) of nickel-affinity purified protein revealed the presence of a nearhomogeneous band of approximately 37 kDa. The identity of the 37 kDa species was verified as rAcpA by proteomic analysis with a molecular mass of 34.6 kDa from the deduced sequence. The dependence of substrate hydrolysis on pH was broad with an optimum observed at 6.0. Kinetic analysis revealed relatively high affinity for PNPP (Km = 90 μM) with Vmax, kcat, and Kcat/Km values of 19.2 pmoles s-1, 4.80 s-1(calculated on the basis of 37 kDa), and 5.30 × 104 M-1s-1, respectively. Sensitivity to a variety of reagents, i.e., detergents, reducing, and chelating agents as well as classic acid phosphatase inhibitors was examined in addition to assessment of hydrolysis of a number of phosphorylated compounds. Removal of phosphate from different phosphorylated compounds is supportive of broad, i.e., 'nonspecific' substrate specificity; although, the enzyme appears to prefer phosphotyrosine and/or peptides containing phosphotyrosine in comparison to serine and threonine. Examination of the primary sequence indicated the absence of signature sequences characteristic of Type A, B, and C nonspecific bacterial acid phosphatases.

Kinase-Inhibitory Nucleoside Derivatives from the Pacific Bryozoan Nelliella nelliiformis

Bracegirdle, Joe,Gordon, Dennis P.,Harvey, Joanne E.,Keyzers, Robert A.

, p. 547 - 551 (2020/03/19)

Marine organisms are a valuable source of bioactive natural products, yet bryozoan invertebrates have been relatively understudied. Herein, we report nelliellosides A and B, new secondary metabolites of the Pacific bryozoan Nelliella nelliiformis, found using NMR-guided isolation. Their structures, including absolute configurations, were elucidated using spectroscopic and chromatographic techniques. Total synthesis of the natural products and four analogues was also achieved, in addition to an assessment of their biological activity, especially kinase inhibition.

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