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18636-98-1

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18636-98-1 Usage

General Description

2-Methylbenzamidine hydrochloride is a chemical compound that consists of a benzamidine group with a methyl substituent and a hydrochloride salt. It is commonly used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. As a strong base, it can also be used in the synthesis of various organic compounds. Additionally, 2-Methylbenzamidine hydrochloride has been studied for its potential antiviral and antitumor activities, making it a potentially important compound in medicinal chemistry research. Overall, this chemical compound has versatile uses in organic synthesis and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 18636-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,3 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18636-98:
(7*1)+(6*8)+(5*6)+(4*3)+(3*6)+(2*9)+(1*8)=141
141 % 10 = 1
So 18636-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2.ClH/c1-6-4-2-3-5-7(6)8(9)10;/h2-5H,1H3,(H3,9,10);1H

18636-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methylbenzamidine hydrochloride

1.2 Other means of identification

Product number -
Other names 2-methylbenzimidamide 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:18636-98-1 SDS

18636-98-1Upstream product

18636-98-1Relevant articles and documents

Catalytic asymmetric hydrogenation of pyrimidines

Kuwano, Ryoichi,Hashiguchi, Yuta,Ikeda, Ryuhei,Ishizuka, Kentaro

supporting information, p. 2393 - 2396 (2015/03/04)

The asymmetric hydrogenation of pyrimidines proceeded with high enantioselectivity (up to 99% ee) using an iridium catalyst composed of [IrCl(cod)]2, a ferrocene-containing chiral diphosphine ligand (Josiphos), iodine, and Yb(OTf)3 (cod=1,5-cyclooctadiene). The chiral catalyst converted various 4-substituted pyrimidines into chiral 1,4,5,6-tetrahydropyrimidines in high yield. The lanthanide triflate is crucial for achieving the high enantioselectivity as well as for activating the heteroarene substrate.

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