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1383677-55-1

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1383677-55-1 Usage

Type of compound

Organic compound

Common uses

Building block or intermediate in the synthesis of pharmaceuticals and agrochemicals

Potential properties

Medicinal (anti-inflammatory, anti-tumor)

Research and development

Used in the development of new drugs

Importance

Important component in the pharmaceutical industry

Additional uses

Reagent in organic synthesis, catalyst in chemical reactions

Check Digit Verification of cas no

The CAS Registry Mumber 1383677-55-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,6,7 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1383677-55:
(9*1)+(8*3)+(7*8)+(6*3)+(5*6)+(4*7)+(3*7)+(2*5)+(1*5)=201
201 % 10 = 1
So 1383677-55-1 is a valid CAS Registry Number.

1383677-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohex-2-en-1-yl 1-methylindazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names Cyclohex-2-en-1-yl 1-methyl-1H-indazole-3-carboxylate

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:1383677-55-1 SDS

1383677-55-1Downstream Products

1383677-55-1Relevant articles and documents

Tetrabutylammonium iodide catalyzed synthesis of allylic ester with tert -butyl hydroperoxide as an oxidant

Shi, Erbo,Shao, Ying,Chen, Shulin,Hu, Huayou,Liu, Zhaojun,Zhang, Jie,Wan, Xiaobing

supporting information; experimental part, p. 3384 - 3387 (2012/08/08)

A metal-free C-H oxidation for the construction of allylic esters has been developed. The use of a commercially available and inexpensive catalyst and oxidant, and readily available starting materials, coupled with the operational simplicity of the reacti

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