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60-27-5 Usage

Description

Creatinine is together with urea, the most widely known "uremic toxin", and is usually assessed when- ever a reduction in kidney function is suspected. This is mainly because creatinine evaluation is cheap, widely accessible and relatively well reflects the renal function. It also forms the basis for estimation of estimated glomerular filtration rate (eGFR) and thus is a major component of all principal eGFR equations.Creatinine, which is nonenzymatically produced from the creatine pool in skeletal muscle, but is also to some extent generated from exogenous creatine present in meat, is the major guanidine compound retained in patients with diminished glomerular filtration rate. Creatinine is routinely determined in plasma or serum as a measure of impairment of renal function and it might be expected that a variety of uremic symptoms correlate with the plasma creatinine level; this does not, however, necessarily imply a causal relationship. In fact, high serum creatinine levels correlate with low mortality in HD patients, presumably because the creatinine generation rate reflects the size of the muscle mass. Creatinine seems to be relatively nontoxic. Large amounts of creatinine have been fed to healthy subjects without any adverse effects and animals also tolerate large doses.

Chemical Properties

white powder

Uses

Different sources of media describe the Uses of 60-27-5 differently. You can refer to the following data:
1. metabolic enhancer
2. Creatinine is the end product of creatine catabolism. Creatinine is a normal constituent of urine. Also found together with creatine in muscle tissues and blood. Creatinine is found in all soils and i n grain seeds and other vegetable matter as well as in certain fish and in crab meat extract.
3. Creatinine levels in blood and urine may be used to calculate the creatinine clearance (CrCl), which reflects the glomerular filtration rate (GFR), an important clinical index of renal function. It is a substrate for creatininase.

Definition

ChEBI: A lactam obtained by formal cyclocondensation of creatine. It is a metabolite of creatine.

Biological Functions

Creatinine is a byproduct of a chemical compound called creatine, which helps muscles get the energy that they need. As a waste product, creatinine is filtered out of the blood by the kidneys and removed from the body in urine.A creatinine test measures the amount of this chemical in either the blood or urine. Creatinine levels can provide an indication of how well the kidneys are working.Creatinine may be measured alone or included in a panel of tests that include other compounds found in the urine or blood.https://labtestsonline.org/tests/creatininehttps://www.kidney.org/atoz/content/what-creatinine

General Description

Creatinine is a breakdown product formed by the degradation of creatine phosphate from muscles. The kidneys extract creatinine from the body by filtering almost all of it from the blood and excreting it in the urine. Serum creatinine is the most commonly used indicator for renal functioning. In chemical synthesis, creatinine is used as a heterocyclic nitrogenous compound that produces electron-rich and highly basic creatinine derivatives.

Purification Methods

Likely impurities are creatine and ammonium chloride. Dissolve it in dilute HCl, then neutralise with ammonia. Recrystallise it from H2O by adding excess of Me2CO. The picrate crystallises from 23volumes of boiling H2O and has m 220-221o(dec). [King J Chem Soc 2377 1930, Beilstein 25 III/IV 2543.]

Check Digit Verification of cas no

The CAS Registry Mumber 60-27-5 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 6 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60-27:
(4*6)+(3*0)+(2*2)+(1*7)=35
35 % 10 = 5
So 60-27-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H7N3O/c1-7-2-3(8)6-4(7)5/h2H2,1H3,(H2,5,6,8)/p+1

60-27-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B23097)  Creatinine, 98%   

  • 60-27-5

  • 10g

  • 223.0CNY

  • Detail
  • Alfa Aesar

  • (B23097)  Creatinine, 98%   

  • 60-27-5

  • 50g

  • 895.0CNY

  • Detail
  • Alfa Aesar

  • (B23097)  Creatinine, 98%   

  • 60-27-5

  • 250g

  • 1908.0CNY

  • Detail
  • Sigma-Aldrich

  • (C4255)  Creatinine  anhydrous, ≥98%

  • 60-27-5

  • C4255-10MG

  • 184.86CNY

  • Detail
  • Sigma-Aldrich

  • (C4255)  Creatinine  anhydrous, ≥98%

  • 60-27-5

  • C4255-10G

  • 208.26CNY

  • Detail
  • Sigma-Aldrich

  • (C4255)  Creatinine  anhydrous, ≥98%

  • 60-27-5

  • C4255-25G

  • 448.11CNY

  • Detail
  • Sigma-Aldrich

  • (C4255)  Creatinine  anhydrous, ≥98%

  • 60-27-5

  • C4255-100G

  • 1,078.74CNY

  • Detail
  • Sigma-Aldrich

  • (C4255)  Creatinine  anhydrous, ≥98%

  • 60-27-5

  • C4255-1KG

  • 5,391.36CNY

  • Detail
  • Sigma-Aldrich

  • (PHR1462)  Creatinine  secondary pharmaceutical standard; traceable to USP

  • 60-27-5

  • PHR1462-1G

  • 791.15CNY

  • Detail
  • USP

  • (1150353)  Creatinine  United States Pharmacopeia (USP) Reference Standard

  • 60-27-5

  • 1150353-100MG

  • 4,647.24CNY

  • Detail
  • Sigma-Aldrich

  • (NIST914A)  Creatinine  NIST® SRM® 914a

  • 60-27-5

  • NIST914A

  • 10,356.84CNY

  • Detail

60-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name creatinine

1.2 Other means of identification

Product number -
Other names Creatinine,heated

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:60-27-5 SDS

60-27-5Synthetic route

C5H8N2O2
1414382-33-4

C5H8N2O2

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
With ammonium hydroxide In neat (no solvent) at 20℃; for 0.5h; Green chemistry;90%
Sarcosine ethyl ester
13200-60-7

Sarcosine ethyl ester

CYANAMID
420-04-2

CYANAMID

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
at 25℃;
N-carbamimidoyl-N-methyl-glycine methyl ester

N-carbamimidoyl-N-methyl-glycine methyl ester

1-methyl-4-nitrosobenzene
623-11-0

1-methyl-4-nitrosobenzene

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
Reaktion des Hydrochlorids;
Phosphocreatine
67-07-2

Phosphocreatine

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
beim Erhitzen von Calcium-kreatinphosphat;
N-carbamimidoyl-N-methyl-glycine methyl ester; hydrochloride
132478-02-5

N-carbamimidoyl-N-methyl-glycine methyl ester; hydrochloride

(E)-3-Ureido-but-2-enoic acid ethyl ester
5435-44-9, 22243-66-9

(E)-3-Ureido-but-2-enoic acid ethyl ester

creatinine
60-27-5

creatinine

N-carbamimidoyl-N-methyl-glycine methyl ester; hydrochloride
132478-02-5

N-carbamimidoyl-N-methyl-glycine methyl ester; hydrochloride

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
beim trocknen Erhitzen;
N-carbamimidoyl-N-methyl-glycine butyl ester; hydrochloride

N-carbamimidoyl-N-methyl-glycine butyl ester; hydrochloride

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
beim trocknen Erhitzen;
cholin hydroxide
123-41-1

cholin hydroxide

A

creatinine
60-27-5

creatinine

B

Creatinine
57-00-1

Creatinine

Conditions
ConditionsYield
Bei der Einw.von Gemischen aus Gehirn- und Leberbrei von Hunden oder Ratten in Gegenwart von Arginin oder Harnstoff;
Bei der Einw.von Gemischen aus Muskel- und Leberbrei von Hunden oder Ratten in Gegenwart von Arginin oder Harnstoff;
acetic acid
64-19-7

acetic acid

Creatinine
57-00-1

Creatinine

creatinine
60-27-5

creatinine

Sarcosine ethyl ester
13200-60-7

Sarcosine ethyl ester

CYANAMID
420-04-2

CYANAMID

guanidine nitrate
113-00-8

guanidine nitrate

creatinine
60-27-5

creatinine

Sarcosine ethyl ester
13200-60-7

Sarcosine ethyl ester

guanidine nitrate
113-00-8

guanidine nitrate

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
at -15℃; Reagiert analog mit dl-Leucin-aethylester, d-Glutaminsaeure-diaethylester und dl-Tyrosin-aethylester;
at -15℃;
ethanol
64-17-5

ethanol

N-carbamimidoyl-N-methyl-glycine methyl ester; hydrochloride
132478-02-5

N-carbamimidoyl-N-methyl-glycine methyl ester; hydrochloride

diethylamine
109-89-7

diethylamine

creatinine
60-27-5

creatinine

ethanol
64-17-5

ethanol

N-carbamimidoyl-N-methyl-glycine butyl ester; hydrochloride

N-carbamimidoyl-N-methyl-glycine butyl ester; hydrochloride

diethylamine
109-89-7

diethylamine

creatinine
60-27-5

creatinine

ethyl 2-(3-methylguanidino)acetate hydrochloride
15366-32-2

ethyl 2-(3-methylguanidino)acetate hydrochloride

diethylamine
109-89-7

diethylamine

benzene
71-43-2

benzene

creatinine
60-27-5

creatinine

formic acid
64-18-6

formic acid

Creatinine
57-00-1

Creatinine

creatinine
60-27-5

creatinine

1-methyl-4-nitrosobenzene
623-11-0

1-methyl-4-nitrosobenzene

Creatinine
57-00-1

Creatinine

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
at 37.5℃; Geschwindigkeit bei verschiedener Konzentration;
at 50.2℃; Geschwindigkeit bei verschiedener Konzentration;
(E)-3-Ureido-but-2-enoic acid ethyl ester
5435-44-9, 22243-66-9

(E)-3-Ureido-but-2-enoic acid ethyl ester

Creatinine
57-00-1

Creatinine

creatinine
60-27-5

creatinine

Creatinine
57-00-1

Creatinine

trichloroacetic acid
76-03-9

trichloroacetic acid

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
Geschwindigkeit;
Creatinine
57-00-1

Creatinine

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
im menschlichen und tierischen Organismus;
at 37 - 38℃; Geschwindigkeit bei Inkubation von Extrakten aus Hirn- und Muskelgeweben;
bei Einw. von Muskelextrakt;
under 3420 Torr; bei 3-stdg. Erhitzen;
creatine

creatine

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
With hydrogenchloride at 30℃; Rate constant;
phosphorocreatine

phosphorocreatine

A

creatinine
60-27-5

creatinine

B

creatine

creatine

Conditions
ConditionsYield
With hydrogenchloride at 30℃; Rate constant; Mechanism; reaction in 18O-enriched water;
phosphorocreatinine

phosphorocreatinine

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
With hydrogenchloride at 30℃; Rate constant;
hydrogenchloride
7647-01-0

hydrogenchloride

Creatinine
57-00-1

Creatinine

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
at 37.5℃; Geschwindigkeit bei verschiedener Konzentration;
at 50.2℃; Geschwindigkeit bei verschiedener Konzentration;
at 120℃; Geschwindigkeit bei verschiedener Konzentration;
water
7732-18-5

water

Creatinine
57-00-1

Creatinine

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
at 100℃;
at 38℃; Geschwindigkeit bei pH 6.0 bis pH 7.5;
Creatinine
57-00-1

Creatinine

aqueous picric acid

aqueous picric acid

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
at 100℃; Geschwindigkeit;
Creatinine
57-00-1

Creatinine

mineral acid

mineral acid

creatinine
60-27-5

creatinine

Phosphocreatine
67-07-2

Phosphocreatine

water
7732-18-5

water

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
at 38℃; Geschwindigkeit der Hydrolyse und der Umwandlung beim pH 6.0 bis 7.5;
at 37℃; Geschwindigkeit der Hydrolyse und der Umwandlung beim pH 1 bis 8;
Phosphocreatine
67-07-2

Phosphocreatine

acid

acid

creatinine
60-27-5

creatinine

Conditions
ConditionsYield
neben der Hydrolyse;
Phosphocreatine
67-07-2

Phosphocreatine

HCl(gas)

HCl(gas)

A

creatinine
60-27-5

creatinine

B

5-phosphono-3-methyl-hydantoic acid

5-phosphono-3-methyl-hydantoic acid

Conditions
ConditionsYield
at 103℃;
creatinine
60-27-5

creatinine

6-nitro-4-oxo-4H-chromene-3-carbaldehyde
42059-80-3

6-nitro-4-oxo-4H-chromene-3-carbaldehyde

2-Imino-1-methyl-5-[1-(6-nitro-4-oxo-4H-chromen-3-yl)-meth-(Z)-ylidene]-imidazolidin-4-one

2-Imino-1-methyl-5-[1-(6-nitro-4-oxo-4H-chromen-3-yl)-meth-(Z)-ylidene]-imidazolidin-4-one

Conditions
ConditionsYield
With boric acid In dimethyl sulfoxide for 0.05h; microwave irradiation;98%
creatinine
60-27-5

creatinine

1-benzylisatin
1217-89-6

1-benzylisatin

1-benzyl-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

1-benzyl-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;98%
creatinine
60-27-5

creatinine

N-ethylisatin
4290-94-2

N-ethylisatin

3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)-1-ethylindolin-2-one

3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)-1-ethylindolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;97%
creatinine
60-27-5

creatinine

1-methyl-1H-indole-2,3-dione
2058-74-4

1-methyl-1H-indole-2,3-dione

3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)-1-methylindolin-2-one

3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)-1-methylindolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;96%
creatinine
60-27-5

creatinine

indole-2,3-dione
91-56-5

indole-2,3-dione

3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;95%
creatinine
60-27-5

creatinine

5-Bromo-1H-indole-2,3-dione
87-48-9

5-Bromo-1H-indole-2,3-dione

5-bromo-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

5-bromo-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;95%
creatinine
60-27-5

creatinine

1-hexyl-2,3-dihydro-1H-indole-2,3-dione
56932-61-7

1-hexyl-2,3-dihydro-1H-indole-2,3-dione

3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)-1-hexylindolin-2-one

3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)-1-hexylindolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;95%
creatinine
60-27-5

creatinine

5-fluoro-1H-indole-2,3-dione
443-69-6

5-fluoro-1H-indole-2,3-dione

C12H11FN4O3

C12H11FN4O3

Conditions
ConditionsYield
With sodium acetate; acetic acid for 0.00833333h; Microwave irradiation; Cooling;94%
creatinine
60-27-5

creatinine

5-fluoro-1H-indole-2,3-dione
443-69-6

5-fluoro-1H-indole-2,3-dione

5-fluoro-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

5-fluoro-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;94%
creatinine
60-27-5

creatinine

5-chloroindole 2,3-dione
17630-76-1

5-chloroindole 2,3-dione

5-chloro-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

5-chloro-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;94%
creatinine
60-27-5

creatinine

N-benzoylisatin
28284-05-1

N-benzoylisatin

1-benzoyl-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

1-benzoyl-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;94%
thiophene-2-carbaldehyde
98-03-3

thiophene-2-carbaldehyde

creatinine
60-27-5

creatinine

5- 2-imino-1-methyl imidazolid-4-one

5- 2-imino-1-methyl imidazolid-4-one

Conditions
ConditionsYield
for 0.0541667h; Irradiation;93%
creatinine
60-27-5

creatinine

2,4,6-Trinitrophenol
88-89-1

2,4,6-Trinitrophenol

C10H8N6O8(2-)*2Na(1+)

C10H8N6O8(2-)*2Na(1+)

Conditions
ConditionsYield
With sodium hydroxide In methanol Heating;92%
creatinine
60-27-5

creatinine

2-(5,7-Bis-benzyloxy-4,6-dimethyl-1H-indol-3-yl)-ethylamine
99053-86-8

2-(5,7-Bis-benzyloxy-4,6-dimethyl-1H-indol-3-yl)-ethylamine

5,7-dihydroxy-4,6-dimethyltryptamine creatinine sulfate
99053-92-6

5,7-dihydroxy-4,6-dimethyltryptamine creatinine sulfate

Conditions
ConditionsYield
With sulfuric acid; hydrogen; palladium on activated charcoal In ethanol under 2068.6 Torr; for 6h; Ambient temperature;92%
creatinine
60-27-5

creatinine

6-Chloro-4-oxo-4H-chromene-3-carbaldehyde
42248-31-7

6-Chloro-4-oxo-4H-chromene-3-carbaldehyde

5-[1-(6-Chloro-4-oxo-4H-chromen-3-yl)-meth-(Z)-ylidene]-2-imino-1-methyl-imidazolidin-4-one

5-[1-(6-Chloro-4-oxo-4H-chromen-3-yl)-meth-(Z)-ylidene]-2-imino-1-methyl-imidazolidin-4-one

Conditions
ConditionsYield
With boric acid In dimethyl sulfoxide for 0.05h; microwave irradiation;92%
creatinine
60-27-5

creatinine

1-[(4-chlorophenyl)carbonyl]-1H-indole-2,3-dione
21591-87-7

1-[(4-chlorophenyl)carbonyl]-1H-indole-2,3-dione

C19H15ClN4O4

C19H15ClN4O4

Conditions
ConditionsYield
With sodium acetate; acetic acid for 0.0111111h; Microwave irradiation; Cooling;92%
creatinine
60-27-5

creatinine

5-nitroisatin
611-09-6

5-nitroisatin

C12H11N5O5

C12H11N5O5

Conditions
ConditionsYield
With sodium acetate; acetic acid for 0.0111111h; Microwave irradiation; Cooling;92%
creatinine
60-27-5

creatinine

indole-2,3-dione
91-56-5

indole-2,3-dione

C12H12N4O3

C12H12N4O3

Conditions
ConditionsYield
With sodium acetate; acetic acid for 0.00555556h; Microwave irradiation; Cooling;92%
creatinine
60-27-5

creatinine

1-phenyl-indole-2,3-dione
723-89-7

1-phenyl-indole-2,3-dione

3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)-1-phenylindolin-2-one

3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)-1-phenylindolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;92%
creatinine
60-27-5

creatinine

1-benzenesulphonyl-2,3-dihydroindole-2,3-dione
58836-98-9

1-benzenesulphonyl-2,3-dihydroindole-2,3-dione

3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)-1-(phenylsulfonyl)indolin-2-one

3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)-1-(phenylsulfonyl)indolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;92%
furfural
98-01-1

furfural

creatinine
60-27-5

creatinine

5--2-imino-1-methyl imidazolid-4-one

5--2-imino-1-methyl imidazolid-4-one

Conditions
ConditionsYield
for 0.0583333h; Irradiation;91%
creatinine
60-27-5

creatinine

vanillin
121-33-5

vanillin

5-<(4-hydroxy-3-methoxyphenyl)methylene> 2-imino-1-methyl imidazolid-4-one
29974-40-1

5-<(4-hydroxy-3-methoxyphenyl)methylene> 2-imino-1-methyl imidazolid-4-one

Conditions
ConditionsYield
for 0.0125h; Irradiation;91%
With sodium acetate; acetic acid for 4h; Reflux;15.2%
creatinine
60-27-5

creatinine

1-(2-bromobenzyl)-1H-indole-3-carboxaldehyde
171734-73-9

1-(2-bromobenzyl)-1H-indole-3-carboxaldehyde

C20H17BrN4O
1207733-64-9

C20H17BrN4O

Conditions
ConditionsYield
With sodium acetate; acetic acid for 0.0111111h; Aldol condensation; Microwave irradiation;91%
creatinine
60-27-5

creatinine

C15H8ClNO3
99448-79-0

C15H8ClNO3

C19H15ClN4O4

C19H15ClN4O4

Conditions
ConditionsYield
With sodium acetate; acetic acid for 0.0111111h; Microwave irradiation; Cooling;91%
creatinine
60-27-5

creatinine

5-chloroindole 2,3-dione
17630-76-1

5-chloroindole 2,3-dione

C12H11ClN4O3

C12H11ClN4O3

Conditions
ConditionsYield
With sodium acetate; acetic acid for 0.0111111h; Microwave irradiation; Cooling;91%
creatinine
60-27-5

creatinine

5-nitroisatin
611-09-6

5-nitroisatin

malononitrile
109-77-3

malononitrile

2-(5-nitro-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)-2-oxoindolin-3-yl)malononitrile

2-(5-nitro-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)-2-oxoindolin-3-yl)malononitrile

Conditions
ConditionsYield
Stage #1: 5-nitroisatin; malononitrile With chloroauric acid In water at 20℃; for 0.25h;
Stage #2: creatinine In water for 0.5h; Reflux; diastereoselective reaction;
91%
creatinine
60-27-5

creatinine

1-acetyl-1H-indole-2,3-dione
574-17-4

1-acetyl-1H-indole-2,3-dione

1-acetyl-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

1-acetyl-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;91%
creatinine
60-27-5

creatinine

5,6-Dibromoisatin
17826-05-0

5,6-Dibromoisatin

5,6-dibromo-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

5,6-dibromo-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one

Conditions
ConditionsYield
With chloroauric acid In water for 0.5h; Aldol Addition; Reflux; diastereoselective reaction;91%
creatinine
60-27-5

creatinine

1-Benzylindole-3-carboxaldehyde
10511-51-0

1-Benzylindole-3-carboxaldehyde

(Z)-2-amino-5-[(1-benzyl-1-H-indol-3-yl)methylene]-1-methyl-1H-imidazol-4(5H)-one
1207733-60-5

(Z)-2-amino-5-[(1-benzyl-1-H-indol-3-yl)methylene]-1-methyl-1H-imidazol-4(5H)-one

Conditions
ConditionsYield
With sodium acetate; acetic acid for 0.0111111h; Aldol condensation; Microwave irradiation;90%
creatinine
60-27-5

creatinine

5-fluoro-1-methylisatin
773-91-1

5-fluoro-1-methylisatin

C13H13FN4O3

C13H13FN4O3

Conditions
ConditionsYield
With sodium acetate; acetic acid for 0.0111111h; Microwave irradiation; Cooling;90%

60-27-5Relevant articles and documents

-

Hongo

, p. 279,289 (1935)

-

-

Lundquist

, p. 98 (1947)

-

A preparation method of creatinine

-

Paragraph 0014; 0028-0042; 0055; 0056, (2019/03/31)

The invention belongs to the technical field of chemical synthesis, in particular relates to a preparation method of creatinine, the method to creatine as the starting material, and containing 2 - 5 carbon of the lower saturated fatty acid reaction. The method of environmental protection, without by-product to produce, almost zero-emission, without refining can be directly used for cardiac muscle protective drug creatine phosphate sodium synthetic.

METHOD FOR PREPARING CREATINE FATTY ESTERS, CREATINE FATTY ESTERS THUS PREPARED AND USES THEREOF

-

Page/Page column 26, (2014/02/16)

The present invention concerns a method for preparing a creatine fatty ester or derivative thereof comprising at least one step consisting in reacting a diprotected creatinine with a molecule bearing at least one alcohol functional group and of formula R'-OH in which R' represents a hydrocarbon radical containing at least 4 carbon atoms. The present invention also concerns particular creatine fatty esters or derivative thereof and medical uses thereof.

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