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Benzene, [(6-methoxy-1-cyclohexen-1-yl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114501-82-5

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114501-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114501-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,5,0 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 114501-82:
(8*1)+(7*1)+(6*4)+(5*5)+(4*0)+(3*1)+(2*8)+(1*2)=85
85 % 10 = 5
So 114501-82-5 is a valid CAS Registry Number.

114501-82-5SDS

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 (6-methoxycyclohexen-1-yl)sulfanylbenzene

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

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:114501-82-5 SDS

114501-82-5Downstream Products

114501-82-5Relevant academic research and scientific papers

1-METHOXY-1-(PHENYLTHIO)CYCLOPROPANES FROM OLEFINS VIA THE PUMMERER REARRANGEMENT

Bhupathy, M.,Cohen, Theodore

, p. 4797 - 4800 (2007/10/02)

The Pummerer rearrangements of cyclopropyl(methoxy)phenylsulfonium salts proceed via sulfur-stabilized carbocations to yield the title compounds.The sulfonium salts were prepared in high yields from olefins via carbene addition, oxidation, and methylation

1-PHENYLTHIO-1-(TRIMETHYLSILOXY)CYCLOPROPANES VIA THE SILA-PUMMERER REARRANGEMENT

Bhupathy, M.,Cohen, Theodore

, p. 4793 - 4796 (2007/10/02)

This first study of the sila-Pummerer rearrangement in a cyclopropane system reveals that several 1-trimethylsiloxy-1-(phenylthio)cyclopropanes can be prepared stereoselectively through putative sulfur-stabilized carbocationic intermediates.

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