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863289-25-2

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863289-25-2 Usage

Indole derivative

A heterocyclic aromatic organic compound with a pyrrole and a benzene ring fused together

Bromoethyl group

A bromine atom attached to an ethyl group (-CH2CH3) attached to the indole ring

Chlorine atom

A chlorine atom attached to the indole ring at the 7-position

Common uses

Chemical research and synthesis, production of pharmaceuticals and agrochemicals

Chemical reactivity

Suitable for reactions involving nucleophilic substitution and other chemical processes

Potential applications

Medicinal chemistry and drug discovery

Check Digit Verification of cas no

The CAS Registry Mumber 863289-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,2,8 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 863289-25:
(8*8)+(7*6)+(6*3)+(5*2)+(4*8)+(3*9)+(2*2)+(1*5)=202
202 % 10 = 2
So 863289-25-2 is a valid CAS Registry Number.

863289-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-bromoethyl)-7-chloro-1H-indole

1.2 Other means of identification

Product number -
Other names 1H-INDOLE,3-(2-BROMOETHYL)-7-CHLORO-

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:863289-25-2 SDS

863289-25-2Downstream Products

863289-25-2Relevant articles and documents

3-Thio-1,2,4-triazoles, novel somatostatin sst2/sst5 agonists

Contour-Galcera, Marie-Odile,Sidhu, Alban,Plas, Pascale,Roubert, Pierre

, p. 3555 - 3559 (2007/10/03)

Novel 3-thio-1,2,4-triazoles have been obtained via a solution-phase parallel synthesis strategy, affording potent non-peptidic human somatostatin receptor subtypes 2 and 5 agonists.

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