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3-(Allylthio)propionic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23246-24-4

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23246-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23246-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,4 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23246-24:
(7*2)+(6*3)+(5*2)+(4*4)+(3*6)+(2*2)+(1*4)=84
84 % 10 = 4
So 23246-24-4 is a valid CAS Registry Number.

23246-24-4SDS

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 3-(Allylthio)propionic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 3-allylsulfanylpropionic 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:23246-24-4 SDS

23246-24-4Downstream Products

23246-24-4Relevant 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

A facile generation of C-S bonds via one-pot, odourless and efficient thia-Michael addition reactions using alkyl, aryl or allyl halides, thiourea and electron-deficient alkenes in wet polyethylene glycol (PEG 200) under mild reaction conditions

Firouzabadi, Habib,Iranpoor, Nasser,Abbasi, Mohammad

experimental part, p. 5293 - 5301 (2009/11/30)

An efficient and odourless synthesis of thia-Michael adducts by the reaction of various organic halides (primary, secondary, tertiary, allylic, and benzylic), structurally diverse electron-deficient alkenes (ketones, esters, and acrylonitrile) and thioure

A Facile Synthesis of Functionalised Organic Sulphides

Singh, Harjit,Batra, Manohar S.

, p. 1111 - 1112 (2007/10/02)

Thioiminium salts and organic halides or Michael acceptors, in the absence of solvent and at ambient temperature, give title compounds in excellent yields.

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