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106000-23-1

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106000-23-1 Usage

Structure

An oxime derivative of 1,7-dimethyl-1H-indole-2,3-dione

Usage

Commonly used in the synthesis of various organic compounds

Potential applications

Organic chemistry and pharmaceuticals (as a building block for the synthesis of complex molecules)

Safety

Handle with caution and follow proper safety protocols in the laboratory

Versatility

Has potential applications in various areas of research and development

Check Digit Verification of cas no

The CAS Registry Mumber 106000-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,0 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106000-23:
(8*1)+(7*0)+(6*6)+(5*0)+(4*0)+(3*0)+(2*2)+(1*3)=51
51 % 10 = 1
So 106000-23-1 is a valid CAS Registry Number.

106000-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,7-Dimethyl-1H-indole-2,3-dione 3-oxime

1.2 Other means of identification

Product number -
Other names -

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:106000-23-1 SDS

106000-23-1Downstream Products

106000-23-1Relevant articles and documents

SYNTHESIS OF SUBSTITUTED THIENOTHIAZOLES AND INDOLOTHIAZOLES

Pinkin, L. D.,Dzyubenko, V. G.,Abramenko, P. I.,Shpileva, I. P.

, p. 345 - 352 (2007/10/02)

Alkylene-, halo-, and aryl-substituted 2-methylthienothiazoles were obtained by the action of phosphorus pentasulfide on the corresponding 2-acetylamino-3-bromo- or 2-acetylamino-3-hydroxythiophenes in an organic solvent with heating. 2-Oximes of halo- and methyl-substituted isatins were converted by reduction and acetylation into 2-hydroxy-3-acetylaminoindoles, from which 2-methylindolo-thiazoles were obtained by the action of phosphorous pentasulfide with heating in xylene.

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