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2-Chloro-N-(4-chlorophenethyl)propan-1-aMine is a chemical compound belonging to the amine class of organic compounds. It is a derivative of propan-1-amine, featuring a chlorine atom attached to the second carbon and a 4-chlorophenethyl group attached to the nitrogen atom. This structural configuration endows the compound with unique properties that can influence its biological activity and interactions within biological systems. Due to its potential hazards and toxicological properties, it is crucial to handle this chemical with care and adhere to proper safety measures.

897926-35-1

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897926-35-1 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-N-(4-chlorophenethyl)propan-1-aMine is utilized as a pharmaceutical intermediate for the synthesis of various medicinal compounds. Its unique structural properties allow it to serve as a building block in the development of drugs with specific therapeutic targets, potentially contributing to the creation of novel treatments for a range of medical conditions.
Used in Research Applications:
In the field of scientific research, 2-Chloro-N-(4-chlorophenethyl)propan-1-aMine is employed as a research chemical. Its distinct structural features make it a valuable tool for studying the interactions between molecules in biological systems, aiding in the understanding of complex biochemical processes and the discovery of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 897926-35-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,7,9,2 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 897926-35:
(8*8)+(7*9)+(6*7)+(5*9)+(4*2)+(3*6)+(2*3)+(1*5)=251
251 % 10 = 1
So 897926-35-1 is a valid CAS Registry Number.

897926-35-1SDS

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-chloro-N-[2-(4-chlorophenyl)ethyl]propan-1-amine

1.2 Other means of identification

Product number -
Other names 1-[[2-(4-CHLOROPHENYL)ETHYL]AMINO]-2-CHLOROPROPANE

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:897926-35-1 SDS

897926-35-1Downstream Products

897926-35-1Relevant articles and documents

8-chloro-1-methyl -2, 3, 4, 5-tetrahydro -1H-3-Benzazepine preparation method

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Paragraph 0042; 0112; 0113, (2017/02/02)

The invention discloses a preparation method of 8-chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzoazatropylidene. The preparation method comprises the following steps: firstly, enabling a compound with a formula (III) to react with aluminium chloride to obtain a compound with a formula (II); and carrying out reduction reaction on the compound with the formula (II) under the combined action of sodium borohydride and aluminium chloride used in the step i) to obtain a compound in a formula (I). The invention also discloses a method for preparing a compound with a formula (V) or a salt thereof. The method comprises the following steps: with chlorobenzyl cyanide and 2-chloropropionic acid as raw materials, reacting under the existence of a carboxylic acid activation reagent to generate a compound in a formula (IV); and carrying out reduction reaction on the compound with the formula (IV) under the action of a reducing agent to obtain the compound with the formula (V). Compared with the prior art, the method disclosed by the invention has the advantages of low cost, convenience for operation, safety of production, high yield and the like.

PROCESSES FOR THE PREPARATION OF LORCASERIN

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, (2016/10/20)

The present invention relates to stable crystalline Form A of lorcaserin hydrochloride of Formula (IA) and processes for its preparation. The invention also relates to processes for the preparation of lorcaserin and pharmaceutically acceptable salts, solvates and hydrates thereof.

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