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1585969-24-9

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1585969-24-9 Usage

General Description

"(R)-2-(1-amino-2-(2,5-dibromophenyl)ethyl)-5-bromopheno" is a chemical compound with a complex structure consisting of two bromine atoms attached to a phenyl ring, and an amino group attached to an ethyl group. (R)-2-(1-amino-2-(2,5-dibromophenyl)ethyl)-5-bromopheno is classified as a substituted phenethylamine, which is a group of psychoactive substances that can have stimulant, hallucinogenic, or entactogenic effects. The presence of bromine atoms in the molecule suggests that it may have unique chemical and physical properties, and could potentially be used in pharmaceutical research or as a starting material for the synthesis of other organic compounds. However, due to the complexity of its structure, (R)-2-(1-amino-2-(2,5-dibromophenyl)ethyl)-5-bromopheno may also pose potential hazards and risks, and should be handled with caution in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 1585969-24-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,5,9,6 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1585969-24:
(9*1)+(8*5)+(7*8)+(6*5)+(5*9)+(4*6)+(3*9)+(2*2)+(1*4)=239
239 % 10 = 9
So 1585969-24-9 is a valid CAS Registry Number.

1585969-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-(1-amino-2-(2,5-dibromophenyl)ethyl)-5-bromophenol

1.2 Other means of identification

Product number -
Other names (R)-2-(1-amino-2-(2,5-dibromophenyl)ethyl)-5-bromopheno

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:1585969-24-9 SDS

1585969-24-9Relevant articles and documents

An Improved Process for the Enantioselective Synthesis of HCV NS5A Inhibitor Elbasvir (MK-8742) Chiral Amine Intermediate

Chapala, Vijaya Lakshmi,Katari, Naresh Kumar,Kerru, Nagaraju,Malavattu, Giri Prasad,Marisetti, Vishnu Murthy,Reddy, Pedavenkatagari Narayana

, p. 932 - 938 (2021/06/26)

Abstract: Large-scale enantioselective synthesis of the chiral amine unit of HCV NS5A inhibitor Elbasvir has been accomplished in six steps, with 55% overall yield. The process includes a highly enantioselective reduction of the NH imine using R-(+)-diphe

PROCESS FOR PREPARING SUBSTITUTED INDOLE COMPOUNDS

-

Page/Page column 0086-0087, (2017/12/27)

The present invention is directed to a process for preparing Substituted Indole Compounds of Formula (I): wherein R1, R2, R3 and R4 are as defined herein. These indole compounds are useful as synthetic intermediates for making inhibitors of HCV NS5A.

Enantioselective synthesis of an HCV NS5a antagonist

Mangion, Ian K.,Chen, Cheng-Yi,Li, Hongmei,Maligres, Peter,Chen, Yonggang,Christensen, Melodie,Cohen, Ryan,Jeon, Ingyu,Klapars, Artis,Krska, Shane,Nguyen, Hoa,Reamer, Robert A.,Sherry, Benjamin D.,Zavialov, Ilia

supporting information, p. 2310 - 2313 (2014/05/20)

A concise, enantioselective synthesis of the HCV NS5a inhibitor MK-8742 (1) is reported. The features of the synthesis include a highly enantioselective transfer hydrogenation of an NH imine and a dynamic diastereoselective transformation. The synthesis of this complex target requires simple starting materials and nine linear steps for completion.

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