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3-Pyridinemethanol, 5-hydroxy-6-methyl-4-(4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridin-4-yl)-(8CI,9CI) is a complex organic compound with the molecular formula C14H16N2O2. It is characterized by a pyridine ring, a hydroxyl group, a methyl group, and a tetrahydro-imidazo[4,5-c]pyridin-4-yl moiety. 3-Pyridinemethanol, 5-hydroxy-6-methyl-4-(4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridin-4-yl)- (8CI,9CI) is a derivative of 3-pyridinemethanol, which is a primary alcohol with a pyridine ring. The presence of the 5-hydroxy-6-methyl group and the tetrahydro-imidazo[4,5-c]pyridin-4-yl group contributes to its unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research. The compound's structure and properties make it a subject of interest for scientists studying the synthesis and reactivity of complex heterocyclic compounds.

4875-52-9

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4875-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4875-52-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4875-52:
(6*4)+(5*8)+(4*7)+(3*5)+(2*5)+(1*2)=119
119 % 10 = 9
So 4875-52-9 is a valid CAS Registry Number.

4875-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(hydroxymethyl)-2-methyl-4-(4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridin-4-yl)pyridin-3-ol

1.2 Other means of identification

Product number -
Other names 3-pyridinemethanol,5-hydroxy-6-methyl-4-(4,5,6,7-tetrahydro-1h-imidazo[4,5-c]pyridin-4-yl)

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:4875-52-9 SDS

4875-52-9Downstream Products

4875-52-9Relevant academic research and scientific papers

STRUCTURE OF THE METAL SCHIFF BASE COMPLEX OF PYRIDOXAL AND HISTIDINE IN SOLUTION

Kondo, Hiroki,Yoshinaga, Hiroyuki,Morita, Kanzi,Sunamoto, Junzo

, p. 31 - 34 (1982)

The cyclization of pyridoxal Schiff base of histidine or histamine is prohibited by metal ions such as Cu2+ and Zn2+.On the basis of a similar extent of metal inhibition for histidine and histamine, it is concluded that an identical Schiff base complex with the imidazole group coordinating to the metal is responsible for the inertness of both substrates.

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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