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15286-68-7

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15286-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15286-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,8 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15286-68:
(7*1)+(6*5)+(5*2)+(4*8)+(3*6)+(2*6)+(1*8)=117
117 % 10 = 7
So 15286-68-7 is a valid CAS Registry Number.

15286-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylsulfanylprop-2-en-1-ol

1.2 Other means of identification

Product number -
Other names (E)-1-phenylthio-1-propen-3-ol

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:15286-68-7 SDS

15286-68-7Relevant articles and documents

CARBON MONOXIDE-RELEASING MOLECULES TRIGGERED BY PHYSIOLOGICAL STIMULI

-

Paragraph 0172; 0180; 0181; 0186, (2019/02/25)

The present invention generally relates to carbon monoxide releasing compounds and compositions, and their use as carbon monoxide prodrugs.

Consecutive Aminolithiation-Carbolithiation of a Linear Aminoalkene Bearing Terminal Vinyl Sulfide Moiety to Give Hydro-indolizine

Yamamoto, Yasutomo,Yamaguchi, Tatsuya,Kaneshige, Atsunori,Hashimoto, Aiko,Kaibe, Sachiho,Miyawaki, Akari,Yamada, Ken-Ichi,Tomioka, Kiyoshi

supporting information, p. 2913 - 2917 (2017/12/14)

Aminolithiation-carbolithiation tandem cyclization of an aminoalkene bearing vinyl sulfide moiety proceeded smoothly using stoichiometric amounts of BuLi. Both aminolithiation and carbo-lithiation were in equilibrium at room temperature, and the stereoche

Regio- and stereoselective copper-catalyzed addition of aromatic and aliphatic thiols to terminal and internal nonactivated alkynes

Trostyanskaya, Inna G.,Beletskaya, Irina P.

experimental part, p. 535 - 540 (2012/04/10)

The CuI-catalyzed regio- and stereoselective hydrothio-lation of terminal and internal alkynes affords (Z) - alkenylsulfides. The following isomerization of the Z-isomers into E-isomers catalyzed by CuI is described. Georg Thieme Verlag Stuttgart · New Yo

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