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2H-Indol-2-one, 1,3-dihydro-1,6-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156136-66-2

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156136-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156136-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,1,3 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 156136-66:
(8*1)+(7*5)+(6*6)+(5*1)+(4*3)+(3*6)+(2*6)+(1*6)=132
132 % 10 = 2
So 156136-66-2 is a valid CAS Registry Number.

156136-66-2SDS

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 1,6-dimethyl-3H-indol-2-one

1.2 Other means of identification

Product number -
Other names 1,6-dimethyl-1,3-dihydroindol-2-one

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:156136-66-2 SDS

156136-66-2Upstream product

156136-66-2Relevant academic research and scientific papers

Copper-Catalyzed Decarboxylative Hydrophosphinylation of α-Acyl-α-Diazoacetates

Zhang, Can,Dong, Chao,Wang, Xin,Shen, Ruwei

supporting information, p. 7440 - 7444 (2020/12/01)

A simple copper-catalyzed decarboxylation–denitrogenation C–P coupling reaction of α-acyl-α-diazoacetates with hydrophosphoryl compounds is reported. The reaction may proceed via a process involving the generation of (diazomethyl)ketones after hydrolysis in the presence of water and the hydrophosphinylation of the copper carbene intermediates. This finding may suggest the potential use of the relatively more readily available α-acyl-α-diazoacetates as replacement of (diazomethyl)ketones in some cases.

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