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Butanoic acid, 3-[(phenylmethyl)thio]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89529-96-4

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89529-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89529-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,2 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89529-96:
(7*8)+(6*9)+(5*5)+(4*2)+(3*9)+(2*9)+(1*6)=194
194 % 10 = 4
So 89529-96-4 is a valid CAS Registry Number.

89529-96-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-benzylsulfanylbutanoate

1.2 Other means of identification

Product number -
Other names 3-benzylsulfanylbutyric acid ethyl ester

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:89529-96-4 SDS

89529-96-4Relevant academic research and scientific papers

Pronounced catalytic effect of a micellar solution of sodium dodecyl sulfate (SDS) on the efficient C-S bond formation via an odorless thia-michael addition reaction through the in situ generation of S-alkylisothiouronium salts

Firouzabadi, Habib,Iranpoor, Nasser,Abbasi, Mohammad

experimental part, p. 755 - 766 (2009/11/30)

A pronounced catalytic effect of sodium dodecyl sulfate (SDS) was observed on the in situ production of 5-alkylisothiouronium salts via the reaction of primary, allyl and benzyl halides with thiourea in SDS droplets .Hydrolysis of the generated Salkylisot

Development of Odorless Thiols and Sulfides and Their Applications to Organic Synthesis

Nishide, Kiyoharu,Ohsugi, Shin-Ichi,Miyamoto, Tetsuo,Kumar, Kamal,Node, Manabu

, p. 189 - 200 (2007/10/03)

Development of new odorless thiols (dodecanethiol, 4-n- heptylphenylmethanethiol, 4-trimethylsilylphenylmethanethiol, 4-trimethylsilylbenzenethiol) and an odorless sulfide (1-methylsulfanyldodecane) and their applications to dealkylation, Michael addition, Swern oxidation, and Corey-Kim oxidation are described.

Synthetic equivalents of benzenethiol and benzyl mercaptan having faint smell: Odor reducing effect of trialkylsilyl group

Nishide, Kiyoharu,Miyamoto, Tetsuo,Kumar, Kamal,Ohsugi, Shin-Ichi,Node, Manabu

, p. 8569 - 8573 (2007/10/03)

Syntheses and odor tests of the trialkylsilylated benzyl mercaptans and benzenethiols have revealed that the trimethylsilyl substituent on the benzene ring has a remarkable effect in reducing the foul smell of the parent benzyl mercaptan and benzenethiol.

ASYMMETRIC SYNTHESES BASED ON 1,3-OXATHIANES. 1. SCOPE OF THE REACTION.

Eliel,Morris-Natschke

, p. 2937 - 2942 (2007/10/02)

The stereoselectivity of the reactions of 2-acyl- and 2-aroyl-4,4,6-trimethyl-1,3-oxathianes and -4,6,6-trimethyl-1,3-oxathianes with organometallic reagents has been studied as a function of the following reaction variables: substitution pattern (4,4,6 o

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