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9-Decen-5-one, 7,7-dimethyl-10-(phenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79681-41-7

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79681-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79681-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,8 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79681-41:
(7*7)+(6*9)+(5*6)+(4*8)+(3*1)+(2*4)+(1*1)=177
177 % 10 = 7
So 79681-41-7 is a valid CAS Registry Number.

79681-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,7-dimethyl-10-phenylsulfanyldec-9-en-5-one

1.2 Other means of identification

Product number -
Other names 9-Decen-5-one,7,7-dimethyl-10-(phenylthio)

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:79681-41-7 SDS

79681-41-7Downstream Products

79681-41-7Relevant academic research and scientific papers

Reactions of 3-Hydroxyvinyl Selenones with Alkoxides. Oxetane Formation and Fragmentation Reactions

Shimizu, Makoto,Ando, Ryoichi,Kuwajima, Isao

, p. 1230 - 1238 (2007/10/02)

3-Hydroxyvinyl phenyl selenones are prepared and their behavior as conjugate addition acceptors has been investigated.As a result, a selenonyl group has been found to activate the C=C bond for conjugate addition of nucleophiles and further to behave as an

Highly Efficient Method for Ethylenic or Acetylenic Ketones via Fragmentation of Hydroxy Vinyl Selenones

Shimizu, Makoto,Ando, Ryoichi,Kuwajima, Isao

, p. 5246 - 5248 (2007/10/02)

Treatment of cyclic 3-hydroxyvinyl selenones with bases at room temperature lea2s to the formation of ethylenic or acetylenic ketones in good yields via 1,4-fragmentaion, where phenylselenonyl group behaves as an excellent nucleofuge.

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