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1341-23-7

Basic Information
CAS No.: 1341-23-7
Name: Pyridinium,3-(aminocarbonyl)-1-b-D-ribofuranosyl-
Article Data: 15
Cas Database
Molecular Structure:
Molecular Structure of 1341-23-7 (Pyridinium,3-(aminocarbonyl)-1-b-D-ribofuranosyl-)
Formula: C11H15 N2 O5
Molecular Weight: 255.25
Synonyms: Pyridinium,3-carbamoyl-1-b-D-ribofuranosyl-(8CI);3-Pyridinecarboxamide, 1-b-D-ribosyl-;Nicotinamide ribonucleoside;Nicotinamide ribose;Nicotinamide riboside;Ribosylnicotinamide;1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyridine-5-carboxamide;nicotinamide-beta-riboside;
EINECS: 1308068-626-2
Density: 1.201g/cm3
Melting Point: N/A
Boiling Point: 646.2 °C at 760 mmHg
Flash Point: 344.6 °C
Solubility: N/A
Appearance: N/A
Hazard Symbols: N/A
Risk Codes: N/A
Safety:
Transport Information: N/A
PSA: 116.25000
LogP: -1.69540
Synthetic route

1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose

98-92-0

nicotinamide

1341-23-7

1-(β-D-ribofuranosyl)-nicotinamide

Conditions
ConditionsYield
Stage #1: 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose With hydrogen bromide; acetic acid In toluene at 0℃; for 2h;
Stage #2: nicotinamide In toluene
Stage #3: With ammonia In methanol at 0℃; Concentration;
86.8%
98-92-0

nicotinamide

13035-61-5

1,2,3,5-tetraacetylribose

1341-23-7

1-(β-D-ribofuranosyl)-nicotinamide

Conditions
ConditionsYield
Stage #1: nicotinamide; 1,2,3,5-tetraacetylribose With trimethylsilyl trifluoromethanesulfonate In acetonitrile at 20℃; for 1.5h;
Stage #2: With methanol at 20℃; for 1h;
Stage #1: nicotinamide; 1,2,3,5-tetraacetylribose With trimethylsilyl trifluoromethanesulfonate In dichloromethane at 30 - 40℃; Large scale;
Stage #2: With potassium carbonate In dichloromethane at 15℃; for 1h; Large scale;

2',3',5'-triacetyl ethyl nicotinate riboside trifluoroacetate

1341-23-7

1-(β-D-ribofuranosyl)-nicotinamide

Conditions
ConditionsYield
With ammonium hydroxide In methanol at 4℃; for 16h;

2',3',5'-triacetyl ethyl nicotinate riboside

1341-23-7

1-(β-D-ribofuranosyl)-nicotinamide

Conditions
ConditionsYield
With ammonia In methanol at 4℃; for 7h;
Stage #1: 2',3',5'-triacetyl ethyl nicotinate riboside With ammonia at -5 - 5℃; for 1h;
Stage #2: With sodium ethanolate In ethanol at -5 - 5℃; for 1h;
1341-23-7

1-(β-D-ribofuranosyl)-nicotinamide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: zirconium(IV) chloride; water / 0.5 h / 80 °C
2: calcium L-ascorbate; water / 48 h / 80 °C
View Scheme
1094-61-7

nicotinamide mononucleotide

1341-23-7

1-(β-D-ribofuranosyl)-nicotinamide

Conditions
ConditionsYield
With water; calcium L-ascorbate at 80℃; for 48h; Reagent/catalyst;

5'-nicotinic acid ethyl ester ribose

1341-23-7

1-(β-D-ribofuranosyl)-nicotinamide

Conditions
ConditionsYield
With ammonia In acetonitrile at -5 - 5℃; for 1h;

1-(2',3',5'-triacetyl-β-D-ribofuranosyl)nicotinamide

1341-23-7

1-(β-D-ribofuranosyl)-nicotinamide

Conditions
ConditionsYield
With methanol at 25℃; for 0.5h; Large scale;0.71 kg
With sodium ethanolate In ethanol at -5 - 5℃; for 1h;
With methanol; sodium methylate at -5 - 0℃; for 5h; Inert atmosphere;8.5 g

nicotinamide riboside glycine

A

1341-23-7

1-(β-D-ribofuranosyl)-nicotinamide

B

56-40-6

glycine

Conditions
ConditionsYield
In aq. buffer pH=7;
13035-61-5

1,2,3,5-tetraacetylribose

1341-23-7

1-(β-D-ribofuranosyl)-nicotinamide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: trimethylsilyl trifluoromethanesulfonate / tetrahydrofuran / 12 h / 0 - 20 °C
2.1: ammonia / 1 h / -5 - 5 °C
2.2: 1 h / -5 - 5 °C
View Scheme
Multi-step reaction with 2 steps
1: trimethylsilyl trifluoromethanesulfonate / tetrahydrofuran / 12 h / 0 - 20 °C
2: sodium ethanolate / ethanol / 1 h / -5 - 5 °C
View Scheme
Multi-step reaction with 4 steps
1: acetonitrile / 8 h / -5 °C / Inert atmosphere
2: sodium hydrogencarbonate; sodium hydroxide / water / 45 °C / Inert atmosphere
3: chloranil / tetrahydrofuran / 0 °C / Inert atmosphere
4: sodium methylate; methanol / 5 h / -5 - 0 °C / Inert atmosphere
View Scheme
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    1341-23-7

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    1341-23-7

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    1341-23-7

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    1.Prompt Goods; 2.Flexible payment terms; 3.Documents & Certificate support. Name: Nicotinamide Riboside Molecular Structure: Formula: C11H16N2O5 Molecular Weight : 256.26 Synonyms: BETA-nicotinamideribose;Beta-NicotinamideRiboside;Nicoti

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    1341-23-7

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    1341-23-7

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  • NICOTINAMIDE RIBOSIDE

  • Casno:

    1341-23-7

    NICOTINAMIDE RIBOSIDE

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  • Nicotinamide Riboside with best price

  • Casno:

    1341-23-7

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    Min.Order: 1 Kilogram

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Specification

The Nicotinamide ribose with cas registry number of 1341-23-7, is also called Pyridinium,3-carbamoyl-1-b-D-ribofuranosyl-(8CI) ;3-Pyridinecarboxamide, 1-b-D-ribosyl- .

Physical properties of Nicotinamide ribose :(1)# of Rule of 5 Violations: 1; (2)#H bond acceptors: 8; (3)#H bond donors: 6; (4)#Freely Rotating Bonds: 9; (5)Polar Surface Area: 153.97 Å2; (6)Enthalpy of Vaporization: 100.16 kJ/mol; (7)Vapour Pressure: 1.39E-17 mmHg at 25°C .

You can still convert the following datas into molecular structure:(1)SMILES:NC(=O)c1cccnc1.O=C[C@H](O)[C@H](O)[C@H](O)CO; (2)InChI:InChI=1/C6H6N2O.C5H10O5/c7-6(9)5-2-1-3-8-4-5;6-1-3(8)5(10)4(9)2-7/h1-4H,(H2,7,9);1,3-5,7-10H,2H2/t;3-,4+,5-/m.0/s1; (3)InChIKey:JQZBTYOVGMGUST-HEEXEHOYBT; (4)Std. InChI:InChI=1S/C6H6N2O.C5H10O5/c7-6(9)5-2-1-3-8-4-5;6-1-3(8)5(10)4(9)2-7/h1-4H,(H2,7,9);1,3-5,7-10H,2H2/t;3-,4+,5-/m.0/s1; (5)Std. InChIKey:JQZBTYOVGMGUST-HEEXEHOYSA-N.