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41009-56-7

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41009-56-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41009-56-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,0 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41009-56:
(7*4)+(6*1)+(5*0)+(4*0)+(3*9)+(2*5)+(1*6)=77
77 % 10 = 7
So 41009-56-7 is a valid CAS Registry Number.

41009-56-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-oxo-3-phenylprop-1-enyl)sulfanyl-1-phenylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names di(benzoylvinyl)sulfide

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:41009-56-7 SDS

41009-56-7Downstream Products

41009-56-7Relevant articles and documents

Synthesis of Novel 1,3,5-Dithiazine Derivatives

Glotova,Protsuk,Albanov,Nakhmanovich,Lopyrev

, p. 789 - 793 (2003)

The reactions of benzoylacetylene, propiolic acid, and methyl propiolate with 2,4-dithiobiuret and 1-substituted and 1,5-disubstituted 2,4-dithiobiurets in glacial AcOH in the presence of HC1O4 or BF3· Et2O were used to ob

Reactions of pyrrole-1-and pyrrole-2-carbodithioates with activated acetylenes

Sobenina,Demenev,Mikhaleva,Elokhina,Stepanova,Mal'kina,Ushakov,Trofimov

, p. 547 - 551 (2007/10/03)

Pyrrole-1-and pyrrole-2-carbodithioates react with activated alkenes (KOH-DMSO, room temperature) along the nucleophilic addition mechanism regio-and stereospecifically to afford pyrrole-1-and pyrrole-2-carbodithioethenes. The adducts of pyrrole-2-carbodi

KETOVINYLIERUNG VON THIOCARBONAMIDEN UND THIOHARNSTOFFEN. ZUR AMBIDENZ DER THIOAMIDFUNKTION

Spitzner, R.,Mielke, D.,Scholz, D.,Schroth, W.,Preiss, A.

, p. 927 - 936 (2007/10/02)

Thiocarbamides and thioureas 1 react as ambident systems with β-chlorovinyl ketones 2 to give the S--salts 3-5.Those obtained from monoprotic 1 undergo deprotonation, yielding isolable S-thioimidateesters or -isothioureas 6 r

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