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29198-41-2

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29198-41-2 Usage

General Description

1,3-Benzothiazol-2-ylmethylamine hydrochloride is a chemical compound with the molecular formula C8H9ClN2S. It is a hydrochloride salt of the amine derivative of benzothiazole, which is a heterocyclic compound containing a thiazole ring fused to a benzene ring. This chemical is used in a variety of applications, including as a building block for the synthesis of pharmaceuticals, pesticides, and other organic compounds. It is also used as a reagent in chemical research and as an intermediate in the production of dyes and pigments. 1,3-Benzothiazol-2-ylmethylamine hydrochloride is a white to off-white crystalline solid that is soluble in water and other polar solvents, and it should be handled and stored according to standard laboratory safety practices.

Check Digit Verification of cas no

The CAS Registry Mumber 29198-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,9 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29198-41:
(7*2)+(6*9)+(5*1)+(4*9)+(3*8)+(2*4)+(1*1)=142
142 % 10 = 2
So 29198-41-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2S.ClH/c9-5-8-10-6-3-1-2-4-7(6)11-8;/h1-4H,5,9H2;1H

29198-41-2SDS

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 1,3-benzothiazol-2-ylmethanamine,hydrochloride

1.2 Other means of identification

Product number -
Other names C-Benzothiazol-2-yl-methylamin,Hydrochlorid

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:29198-41-2 SDS

29198-41-2Relevant articles and documents

Catalytic Staudinger Reduction at Room Temperature

Lenstra, Danny C.,Wolf, Joris J.,Mecinovi?, Jasmin

, p. 6536 - 6545 (2019/05/24)

We report an efficient catalytic Staudinger reduction at room temperature that enables the preparation of a structurally diverse set of amines from azides in excellent yields. The reaction is based on the use of catalytic amounts of triphenylphosphine as a phosphine source and diphenyldisiloxane as a reducing agent. Our catalytic Staudinger reduction exhibits a high chemoselectivity, as exemplified by reduction of azides over other common functionalities, including nitriles, alkenes, alkynes, esters, and ketones.

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