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85124-16-9

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85124-16-9 Usage

General Description

5-Chloro-1H-indole-2,3-dione 3-oxime is a chemical compound that is a derivative of the indole-2,3-dione molecule. It contains a chlorine atom at the 5-position of the indole ring and an oxime group at the 3-position. 5-Chloro-1H-indole-2,3-dione 3-oxime has potential uses in the pharmaceutical industry, particularly in the development of new drugs and treatments. It may have biological activity and could be investigated for its potential as a therapeutic agent. Additionally, it may serve as a useful building block for the synthesis of other chemical compounds. Overall, 5-Chloro-1H-indole-2,3-dione 3-oxime is a potentially important chemical with various applications in the field of chemistry and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 85124-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,2 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85124-16:
(7*8)+(6*5)+(5*1)+(4*2)+(3*4)+(2*1)+(1*6)=119
119 % 10 = 9
So 85124-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H5ClN2O2/c9-4-1-2-6-5(3-4)7(11-13)8(12)10-6/h1-3,13H,(H,10,11,12)

85124-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-3-(hydroxyamino)indol-2-one

1.2 Other means of identification

Product number -
Other names 5-chloro-indoline-2,3-dione-3-oxime

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:85124-16-9 SDS

85124-16-9Relevant articles and documents

Synthesis of isatin 3-oximes from 2-nitroacetanilides

Kearney,Harris,Jackson,Joule

, p. 769 - 772 (2007/10/02)

2-Nitroacetanilides, prepared by alkaline hydrolysis of 1-arylamino-1-methylthio-2-nitroethenes, are converted into isatin (1H-indole-2,3-dione) 3-oximes by treatment with concentrated sulfuric acid or trifluoromethanesulfonic acid at room temperature.

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