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1-Butanol, 3-methyl-4-(phenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88408-80-4

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88408-80-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88408-80-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,0 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88408-80:
(7*8)+(6*8)+(5*4)+(4*0)+(3*8)+(2*8)+(1*0)=164
164 % 10 = 4
So 88408-80-4 is a valid CAS Registry Number.

88408-80-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-4-phenylsulfanylbutan-1-ol

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:88408-80-4 SDS

88408-80-4Relevant academic research and scientific papers

Fenton-Inspired C-H Functionalization: Peroxide-Directed C-H Thioetherification

Groendyke, Brian J.,Modak, Atanu,Cook, Silas P.

, p. 13073 - 13091 (2019/10/10)

Substoichiometric iron mediates the thioetherification of unactivated aliphatic C-H bonds directed by resident silylperoxides. Upon exposure to a catalytic amount of iron(II) triflate, TIPS-protected peroxides bearing primary, secondary, and tertiary C-H sites undergo chemoselective thioetherification of remote C-H bonds with diaryl disulfides. The reaction demonstrates a broad substrate scope and functional group tolerance without the use of any noble metal additives. Mechanistic experiments suggest that the reaction proceeds through 1,5-H atom abstraction by a hydroxyl radical generated with iron.

Stereoselective synthesis of the macrolactone core of (+)-neopeltolide

Raghavan, Sadagopan,Samanta, Pradip Kumar

, p. 2346 - 2349 (2012/07/01)

A stereoselective synthesis of the macrolactone core of the potent anticancer agent neopeltolide is disclosed. The key steps of the synthesis include asymmetric allylation using Krische' protocol, conjugate reduction using MacMillan's methodology, and an

PREPARATION OF CHIRAL C5-BUILDING BLOCKS FOR TERPENE SYNTHESIS BY BAKERS' YEAST REDUCTION OF SULFUR-FUNCTIONALIZED PRENYL DERIVATIVES

Sato, Toshio,Hanayama, Kyoko,Fujisawa, Tamotsu

, p. 2197 - 2200 (2007/10/02)

Enantioselective hydrogenation of several α,β-unsaturated aldehydes and allylic alcohols of sulfur-functionalized prenyl derivatives with bakers' yeast gave bifunctional chiral (S)- and (R)-C5-building blocks for terpene synthesis with high enantiomeric e

Certain polyprenyl intermediates

-

, (2008/06/13)

Novel polyprenyl compounds have the general formula: STR1 represents a cis-isoprene unit, n is an integer of 11-19, Z1 is --CH2 OH or a functional precursor thereof, and either one of R1 and R2 is a hydrogen ato

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