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1-Propanol, 3-[(4-methylphenyl)sulfinyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87943-27-9

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87943-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87943-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,4 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87943-27:
(7*8)+(6*7)+(5*9)+(4*4)+(3*3)+(2*2)+(1*7)=179
179 % 10 = 9
So 87943-27-9 is a valid CAS Registry Number.

87943-27-9SDS

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 3-(4-methylphenyl)sulfinylpropan-1-ol

1.2 Other means of identification

Product number -
Other names 3-hydroxypropyl p-tolyl sulfone

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:87943-27-9 SDS

87943-27-9Downstream Products

87943-27-9Relevant academic research and scientific papers

The remarkable effect of methanol on sulfide photooxidations. Evidence for its dual reactivity

Clennan, Edward L.,Yang, Kang

, p. 1697 - 1700 (2007/10/02)

The addition of small amounts of methanol to photooxidation mixtures of sulfides dramatically enhances sulfone in preference to sulfoxide formation. High concentrations of methanol on the other hand have the opposite effect of promoting sulfoxide in prefe

Remote Participation during Photooxidation at Sulfur. Eidence for Sulfurane Intermediates

Clennan, E. L.,Yang, Kang

, p. 4477 - 4487 (2007/10/02)

The photooxidations of geminally substituted γ-hydroxy sulfides results in formation of unusual oxidative elimination products.Detailed spectral data and the independent synthesis of a close analogue provide compelling evidence for the structures of these

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