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3-Cyclohexene-1-acetic acid, 1-ethyl-2-oxo-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103012-99-3

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103012-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103012-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,0,1 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103012-99:
(8*1)+(7*0)+(6*3)+(5*0)+(4*1)+(3*2)+(2*9)+(1*9)=63
63 % 10 = 3
So 103012-99-3 is a valid CAS Registry Number.

103012-99-3SDS

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 methyl 2-(1-ethyl-2-oxocyclohex-3-en-1-yl)acetate

1.2 Other means of identification

Product number -
Other names 3-Cyclohexene-1-acetic acid,1-ethyl-2-oxo-,methyl ester

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:103012-99-3 SDS

103012-99-3Relevant academic research and scientific papers

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid

-

, (2008/06/13)

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation and use are disclosed. The compounds are useful analgesic and antiinflammatory agents.

1,4-DIASTEREOSELECTIVITY IN THE ADDITION OF ALLYLSTANNANES TO 1-ALKYL-2-OXOCYCLOHEX-3-ENEACETIC ACID METHYL ESTERS

Mobilio, Dominick,Lange, Barbara De

, p. 1483 - 1486 (2007/10/02)

Cyclohexanones 1 were allowed to react with allyltrimethylsilane and three allyltributylstannanes in the presence of titanium tetrachloride.Products 2 and 3 were formed in ratios ranging from 7:1 to 26:1 (2:3).Ratios resulting from the use of other Lewis acids support 4 as an intermediate which accounts for the observed stereoselectivity.

Process for preparing substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid

-

, (2008/06/13)

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation and use are disclosed. The compounds are useful analgesic and antiinflammatory agents.

Production of substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives

-

, (2008/06/13)

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation. The compounds are useful analgesic and anti-inflammatory agents.

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid, compositions and use

-

, (2008/06/13)

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation and use are disclosed. The compounds are useful analgesic and antiinflammatory agents.

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid, compositions and use

-

, (2008/06/13)

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation and use are disclosed. The compounds are useful analgesic and antiinflammatory agents.

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives, compositions and use

-

, (2008/06/13)

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation and use are disclosed. The compounds are useful analgesic and antiinflammatory agents.

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