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85052-88-6

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85052-88-6 Usage

General Description

2-(4-Chlorobenzenesulfonyl)-ethylamine hydrochloride is a chemical compound that is derived from 4-chlorobenzenesulfonyl chloride and ethylamine. It is often used as a reagent in the synthesis of various pharmaceutical and organic compounds. 2-(4-CHLOROBENZENESULFONYL)-ETHYLAMINE HYDROCHLORIDE is a hydrochloride salt, which means it is in a stable and easily solubilized form, making it suitable for use in a variety of chemical reactions. Its structure and properties make it useful for a range of applications in organic chemistry, particularly in the production of drugs and other complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 85052-88-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,5 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85052-88:
(7*8)+(6*5)+(5*0)+(4*5)+(3*2)+(2*8)+(1*8)=136
136 % 10 = 6
So 85052-88-6 is a valid CAS Registry Number.

85052-88-6SDS

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-(4-chlorophenyl)sulfonylethanamine,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-[(4-Chlorophenyl)sulfonyl]ethanamine,monohydrochloride

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:85052-88-6 SDS

85052-88-6Relevant articles and documents

2-(Arylthio)ethanamines and &α-(Arylthio)propionamides with Antidepressant Activity

Nair, M. D.,David, J.,Nagarajan, K.

, p. 940 - 947 (2007/10/02)

Reaction of aziridine with thiophenols affords 2-arylthioethanamines; with 2-methylaziridine, ring opening occurs regiospecifically to provide 1-arylthio-2-propanamines.The structure of one member of this group, 1-(4-chlorophenylthio)-2-propanamine (7), has been proved by other unambiguous syntheses. 7 and isomer 12 arise from the alkylation of 4-chlorothiophenol with 2-chloropropylamine as well as from the displacement of the tosyl group in 1-(4-chlorophenylthio)-2-tosyloxypropane (13).Alkylation of 4-chlorothiophenol with α-chloropropionamide affords 11 which leads to 12 on LAH reduction.Ethanamines and propanamines are converted into guanidines, amides, ureas and thioureas.Many arylthioethanamines, e.g. 7, 22, 28, 38 and 39 (as HCl salts) and α-arylthiopropionamides, e.g. 11, 86, 91, 93 and 96 exhibit good activity in the DOPA potentiation and reserpine antagonism tests.Among these, 7 HCl is the most potent and does not inhibit rat brain MAO activity.In clinical trials, C 2998-Go compares favourably with imipramine.

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