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3-Methyl-3H-imidazo[4,5-c]pyridine is a chemical compound with the molecular formula C7H7N3. It is a heterocyclic aromatic compound, specifically a methylated derivative of imidazo[4,5-c]pyridine. 3-Methyl-3H-imidazo[4,5-c]pyridine is known for its potential mutagenicity and has been classified as a possible human carcinogen by the International Agency for Research on Cancer (IARC). It is formed as a byproduct during the cooking process, particularly when meats are grilled or smoked at high temperatures. The compound has been found in various food products, including char-grilled and smoked meats, and has been the subject of research to understand its impact on human health. Due to its potential health risks, there is ongoing work to develop methods for reducing its formation in food products.

7322-04-5

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7322-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7322-04-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,2 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7322-04:
(6*7)+(5*3)+(4*2)+(3*2)+(2*0)+(1*4)=75
75 % 10 = 5
So 7322-04-5 is a valid CAS Registry Number.

7322-04-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylimidazo[4,5-c]pyridine

1.2 Other means of identification

Product number -
Other names 3-methylimidazo<4,5-c>pyridine

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:7322-04-5 SDS

7322-04-5Downstream Products

7322-04-5Relevant academic research and scientific papers

Copper- and palladium-catalyzed amidation reactions for the synthesis of substituted imidazo[4,5-c]pyridines

Wilson, Robert J.,Rosenberg, Adam J.,Kaminsky, Lauren,Clark, Daniel A.

, p. 2203 - 2212 (2014/04/03)

Imidazo[4,5-c]pyridines were synthesized in three steps utilizing a palladium-catalyzed amidation/cyclization strategy. N-Aryl substrates were synthesized using copper-catalyzed amidation of 3-amino-N-Boc-4-chloropyridine. Complementary protocols for the selective chlorination of imidazo[4,5-c] pyridines at the C2 and C7 positions were also developed.

NEW CYCLIZATION REACTIONS OF 3-DIALKYLAMINO-4-AMINOPYRIDINES UNDER CONDITIONS OF NITRATION

Miura, Yutaka,Takaku, Sakae,Nawata, Yoshikaru,Hamana, Masatomo

, p. 1491 - 1495 (2007/10/02)

Treatment of 3-dialkylamino-4-aminopyridines (1) with nitric and sulfuric acids affords imidazopyridine derivatives (2,3 and 4) and 1,2,3-triazolopyridine 2-oxides (5) by cyclization reaction of the corresponding 4-nitroaminopyridines.

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