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Allyl dithiopropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41830-43-7

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41830-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41830-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,3 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41830-43:
(7*4)+(6*1)+(5*8)+(4*3)+(3*0)+(2*4)+(1*3)=97
97 % 10 = 7
So 41830-43-7 is a valid CAS Registry Number.

41830-43-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name prop-2-enyl propanedithioate

1.2 Other means of identification

Product number -
Other names Allyl propanedithioate

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:41830-43-7 SDS

41830-43-7Downstream Products

41830-43-7Relevant academic research and scientific papers

GRIGNARD REAGENTS AS POWDERS : PREPARATION AND REACTIVITY

Boudin, Alain,Cerveau, Genevieve,Chuit, Claude,Corriu, Robert J.P.,Reye, Catherine

, p. 171 - 180 (2007/10/02)

The TDA-1 chelating agent is able to complex Grignard reagents.This complexation leads to powders.The preparation is general and the complexes "RMgX/TDA-1" are easily prepared from every type of Grignard reagents.These solids are stable under nitrogen and can be titrated and used as Grignard reagents.The study of their chemical reactivity shows a behaviour comparable to that of conventional Grignard reagents, the rate of reactions however being decreased.Selective addition onto a mixture of aldehyde and ketone is possible.Interestingly the reactions can be performed in hydrocarbon solvents (toluene, light petroleum, cyclohexane).

Synthesis of Dithioic Acid Esters by a Mitsunobu-Type Reaction of Alkanedithioic Acids and Alcohols

Kpegba, Kafui,Metzner, Patrick

, p. 137 - 139 (2007/10/02)

Alcohols react with dithioic acids in the presence of the complex of diisopropyl azodicarboxylate and triphenylphosphine to give various dithioic acid esters, via a Mitsunobu-type reaction.

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