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21636-09-9

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21636-09-9 Usage

General Description

2-Methylnicotinic Acid Hydrochloride is a chemical compound often used in biochemical and pharmaceutical research. It belongs to the family of Pyridines and derivatives. As a hydrochloride, it exists as a water-soluble, hydrochloric acid salt of 2-methylnicotinic acid, characterized by a strong acidic nature. It appears as a white or off-white crystalline powder, presenting no significant risk of toxicity. Its precise usage can vary, but it typically falls within the realm of laboratory synthesis and drug development. The compound's molecular formula is C7H8ClNO2, and it is often associated with various molecular functions and biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 21636-09-9 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 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21636-09:
(7*2)+(6*1)+(5*6)+(4*3)+(3*6)+(2*0)+(1*9)=89
89 % 10 = 9
So 21636-09-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO2.ClH/c1-5-6(7(9)10)3-2-4-8-5;/h2-4H,1H3,(H,9,10);1H

21636-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylpyridine-3-carboxylic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-methylpyridine-3-carboxylic Acid Hydrochloride

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:21636-09-9 SDS

21636-09-9Downstream Products

21636-09-9Relevant articles and documents

DIBENZOTHIOPHENE DERIVATIVES AS DNA- PK INHIBITORS

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Page/Page column 67, (2010/12/26)

Compound formula I: wherein: X1 and X2 may be either (a) C and O, (b) N and N, or (c) C and NH, where the dotted bonds represents a double bond in the appropriate location; R1 and R2 are independently selected from hydrogen, an optionally substituted C1-7 alkyl group, an optionally substituted C3-20 heterocyclyl group, or an optionally substituted C5-20 aryl group, or may together form, along with the nitrogen atom to which they are attached, an optionally substituted heterocyclic ring having from 4 to 8 ring atoms; RN1 is selected from hydrogen and an optionally substituted C1-4 alkyl group; RC1 is selected from an optionally substituted C1-7 alkyl group, an optionally substituted C3-20 heterocyclyl group, or an optionally substituted C5-20 aryl group; or RN1 and RC1 may together form an optionally substituted C2-4 alkylene group.

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