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3-Hydroxy-3-phenylpropenedithioic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13636-68-5

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13636-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13636-68-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,3 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13636-68:
(7*1)+(6*3)+(5*6)+(4*3)+(3*6)+(2*6)+(1*8)=105
105 % 10 = 5
So 13636-68-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H10OS2/c1-13-10(12)7-9(11)8-5-3-2-4-6-8/h2-7,12H,1H3

13636-68-5SDS

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 (E)-3-methylsulfanyl-1-phenyl-3-sulfanylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-Propene(dithioic) acid,methyl 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:13636-68-5 SDS

13636-68-5Relevant academic research and scientific papers

Spontaneous Resolution upon Crystallization and Preferential Induction of Chirality in a Discrete Tetrahedral Zinc(II) Complex Comprised of Achiral Precursors

Yadav, Chote Lal,Rajput, Gunjan,Bisht, Kamal Kumar,Drew, Michael G. B.,Singh, Nanhai

, p. 14449 - 14456 (2019)

A pair of enantiomeric tetrahedral complexes (Λ-[Zn(L)2] and Δ-[Zn(L)2]) comprised of the achiral ligand methyl-3-hydroxy-3-phenyl-2-propenedithioate (L) have been synthesized by spontaneous resolution. Two chiral inducers, viz., d-(

Catalytic activity of new heteroleptic [Cu(PPh3)2(β-oxodithioester)] complexes: Click derived triazolyl glycoconjugates

Kumari, Kavita,Singh, Anoop S.,Manar, Krishna K.,Yadav, Chote Lal,Tiwari, Vinod K.,Drew, Michael G.B.,Singh, Nanhai

, p. 1166 - 1176 (2019)

A series of four new and two known luminescent heteroleptic Cu(i) complexes of the form [Cu(PPh3)2(β-oxodithioester)] (β-oxodithioester = methyl-3-hydroxy-3-(2-furyl)-2-propenedithioate L1 1, methyl-3-hydroxy-3-(2-thienyl)-2-propened

Et3N mediated synthesis of polysubstituted thiophenes from α-oxo ketene dithioacetals

Kan, Xiaoli,Yang, Xiaobing,Hu, Fangzhong,Wang, Yang,Liu, Ying,Zou, Xiaomao,Li, Hengyu,Li, Hao,Zhang, Qichun

, p. 6198 - 6201 (2015/10/28)

In this Letter, an efficient synthetic route to prepare polysubstituted thiophene derivatives was achieved via the Et3N-mediated (Claisen) rearrangement reaction from α-oxo S-methyl-S-propargyl ketenes, which were obtained through alkylation of

Half-sandwich titanium complexes with β-oxodithioester ligands

Mancilla-González, María Del Carmen,Jancik, Vojtech,Martínez-Otero, Diego,Moya-Cabrera, Mónica,García-Orozco, Iván

, p. 35 - 41 (2015/02/19)

The reaction of CpTiCl3with HLx[HLx= methyl 3-(4′-X-phenyl)-3-hydroxy-2-propenedithioate ligands; X = H(1), Me(2), OMe(3), Cl(4), Br(5)] in the presence of NEt3yielded the corresponding half-sandwich complexes T

An expedient route to highly functionalized 2H-chromene-2-thiones via ring annulation of β-oxodithioesters catalyzed by InCl3 under solvent-free conditions

Verma, Rajiv Kumar,Verma, Girijesh K.,Raghuvanshi, Keshav,Singh, Maya Shankar

experimental part, p. 584 - 589 (2011/03/18)

A convenient and one-pot synthesis of 3-aroyl/heteroaroyl-2H-chromene-2- thiones and benzo[f]2H-chromene-2-thiones has been developed by the condensation of β-oxodithioesters and salicylaldehydes/α-hydroxynaphthaldehydes in the presence of indium trichlor

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