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3-(butylthio)propionaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19378-51-9

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19378-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19378-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,7 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19378-51:
(7*1)+(6*9)+(5*3)+(4*7)+(3*8)+(2*5)+(1*1)=139
139 % 10 = 9
So 19378-51-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H14OS/c1-2-3-6-9-7-4-5-8/h5H,2-4,6-7H2,1H3

19378-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-butylsulfanylpropanal

1.2 Other means of identification

Product number -
Other names 3-Butylmercapto-propionaldehyd

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:19378-51-9 SDS

19378-51-9Relevant academic research and scientific papers

In situ generation of n-butanethiol and its reaction with electron-deficient olefines

Gariani, Rogerio A.,Santos, Alcindo A. Dos,Comasseto, Joao V.

, p. 789 - 795 (2008/09/16)

n-Butanethiol is generated in situ by sequential addition of n-butyllithium and water to elemental sulfur. The n-butanethiol formed was reacted with electron-deficient olefines to give Michael-type addition products in good yields. The method avoids the manipulation of the bad-smelling n-butanethiol. Copyright Taylor & Francis Group, LLC.

Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides

Comasseto, Jo?o V.,Gariani, Rogério A.,Princival, Jefferson L.,Dos Santos, Alcindo A.,Zinn, Fabiano K.

, p. 2929 - 2936 (2008/12/21)

Alkanethiols, selenols and tellurols are generated in situ by reaction of elemental sulfur, selenium and tellurium with commercial alkyllithiums, followed by reaction with deoxygenated water. The alkanechalcogenols react in situ with activated olefins in a Michael-type addition reaction.

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