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4-methyl-4-(phenylsulfanyl)hept-6-en-3-one is a complex organic compound with the molecular formula C14H18OS. It features a hept-6-en-3-one backbone, which consists of a seven-carbon chain with a triple bond between the sixth and seventh carbon atoms and a ketone group (carbonyl) at the third position. The molecule also contains a methyl group attached to the fourth carbon and a phenylsulfanyl group, which is a benzene ring with a sulfur atom attached to the fourth carbon. 4-methyl-4-(phenylsulfanyl)hept-6-en-3-one is characterized by its unique structure and potential applications in the synthesis of various pharmaceuticals and agrochemicals.

55834-35-0

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55834-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55834-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,3 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55834-35:
(7*5)+(6*5)+(5*8)+(4*3)+(3*4)+(2*3)+(1*5)=140
140 % 10 = 0
So 55834-35-0 is a valid CAS Registry Number.

55834-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-4-phenylsulfanylhept-6-en-3-one

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

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More Details:55834-35-0 SDS

55834-35-0Downstream Products

55834-35-0Relevant academic research and scientific papers

Synthesis of Functionalized β-Keto Arylthioethers by the Aryne Induced [2,3] Stevens Rearrangement of Allylthioethers

Thangaraj, Manikandan,Gaykar, Rahul N.,Roy, Tony,Biju, Akkattu T.

, p. 4470 - 4476 (2017/04/28)

A mild and transition-metal-free synthesis of β-keto arylthioethers has been developed by the aryne triggered [2,3] Stevens rearrangement of allylthioethers. The key sulfur ylide intermediate for the rearrangement was formed by the S-arylation of allylthi

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