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1-Acetyl-5-broMo-6-chloro-1H-indol-3-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108847-96-7

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108847-96-7 Usage

Chemical Properties

Yellow to brown powder

Check Digit Verification of cas no

The CAS Registry Mumber 108847-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,8,4 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108847-96:
(8*1)+(7*0)+(6*8)+(5*8)+(4*4)+(3*7)+(2*9)+(1*6)=157
157 % 10 = 7
So 108847-96-7 is a valid CAS Registry Number.

108847-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Acetyl-5-bromo-6-chloro-1H-indol-3-yl acetate

1.2 Other means of identification

Product number -
Other names Ethynyl Estradiol 3-Acetate

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:108847-96-7 SDS

108847-96-7Relevant academic research and scientific papers

5-bromo-6-chloro-3-indolyl caprylate synthesis method

-

, (2017/09/01)

The invention discloses a 5-bromo-6-chloro-3-indolyl caprylate synthesis method, which is characterized in that 4-chloro-2-aminobenzoic acid and N-bromosuccinimide are subjected to a bromination reaction to obtain 5-bromo-4-chloro-2-aminobenzoic acid, 5-b

An improved synthesis of 1-acetyl-1H-indol-3-yl acetates

Rodriguez-Dominguez, Juan C.,Balbuzano-Deus, Alexander,Lopez-Lopez, Miguel A.,Kirsch, Gilbert

, p. 273 - 275 (2008/03/14)

(Chemical Equation Presented) An efficient two steps procedure for the synthesis of 1-acetyl-1H-indol-3-yl acetates, starting from 2-chlorobenzoic acids, was developed and in general, moderate to good yields were obtained.

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