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2-Butenal, 3-methyl-2-(phenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89005-38-9

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89005-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89005-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,0 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89005-38:
(7*8)+(6*9)+(5*0)+(4*0)+(3*5)+(2*3)+(1*8)=139
139 % 10 = 9
So 89005-38-9 is a valid CAS Registry Number.

89005-38-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-2-phenylsulfanylbut-2-enal

1.2 Other means of identification

Product number -
Other names 3-methyl-2-phenylsulfanyl-crotonaldehyde

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:89005-38-9 SDS

89005-38-9Downstream Products

89005-38-9Relevant academic research and scientific papers

Alkyl-and arylsulfanyl-substituted unsaturated carbonyl compounds

Kondrashov, Evgeniy V.,Romanov, Alexey R.,Ushakov, Igor A.,Rulev, Alexander Yu.

, p. 18 - 33 (2017/01/17)

A method for the synthesis of captodative sulfanyl enals, enones and enoates via nucleophilic vinylic substitution of corresponding halogen-bearing derivatives has been developed. The one-pot treatment of the haloenoates, haloenones or haloenals with thiols in the presence of organic base leads either to vicinal dithiosubstituted carbonyl-bearing compound or captodative systems with good to excellent yield. The major reaction direction strongly depends on the type of base used.

Chemistry of Allene Sulphoxides: Novel Transformations of Acetylenic Alcohols

Cutting, Ian,Parsons, Philip J.

, p. 1209 - 1210 (2007/10/02)

The preparation and reactions of allenes derived from 1-phenylthio substituted acetylenic alcohols are described; this chemistry offers new routes to allenyl sulphides, acyl anion equivalents, and substituted unsaturated aldehydes.

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