Cas 21634-29-7,4-(3-hydroxy-5-hydroxymethyl-2-methyl-4-pyridyl)-4,5,6,7-tetrahydropyrido<3,4-d>imidazole-6-carboxylic acid

21634-29-7

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Basic information

Product Name: 4-(3-hydroxy-5-hydroxymethyl-2-methyl-4-pyridyl)-4,5,6,7-tetrahydropyrido<3,4-d>imidazole-6-carboxylic acid
Synonyms:
CAS NO:21634-29-7
Molecular Formula:
Molecular Weight: 304.305
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-(3-hydroxy-5-hydroxymethyl-2-methyl-4-pyridyl)-4,5,6,7-tetrahydropyrido<3,4-d>imidazole-6-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: 4-(3-hydroxy-5-hydroxymethyl-2-methyl-4-pyridyl)-4,5,6,7-tetrahydropyrido<3,4-d>imidazole-6-carboxylic acid(21634-29-7)
EPA Substance Registry System: 4-(3-hydroxy-5-hydroxymethyl-2-methyl-4-pyridyl)-4,5,6,7-tetrahydropyrido<3,4-d>imidazole-6-carboxylic acid(21634-29-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 21634-29-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 21634-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,3 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21634-29:
(7*2)+(6*1)+(5*6)+(4*3)+(3*4)+(2*2)+(1*9)=87
87 % 10 = 7
So 21634-29-7 is a valid CAS Registry Number.

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21634-29-7Relevant academic research and scientific papers

Coordination Modes of Histidine. 2. Stereochemistry of the Reaction between Histidine Derivatives and Pyridoxal Analogues. Conformational Properties of Zinc(II) Complexes of Histidine Schiff Bases

Casella, Luigi,Gullotti, Michele

, p. 6338 - 6347 (2007/10/02)

Pyridoxal reacts with L-histidine, L-histidine methyl ester, histamine and Nτ-methylhistamine to form 4,5,6,7-tetrahydropyridoimidazole compounds through the formation of Schiff base intermediates.The 4,6-trans isomers of the products ar

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