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24165-03-5

24165-03-5

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24165-03-5 Usage

Chemical Properties

Yellow Solid

Uses

Intermediate in the preparation of precursors for cyclic polysulfides.

Check Digit Verification of cas no

The CAS Registry Mumber 24165-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,6 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24165-03:
(7*2)+(6*4)+(5*1)+(4*6)+(3*5)+(2*0)+(1*3)=85
85 % 10 = 5
So 24165-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H15ClS/c20-21-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H

24165-03-5 Well-known Company Product Price

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  • TCI America

  • (T1237)  Triphenylmethanesulfenyl Chloride  >96.0%(HPLC)(T)

  • 24165-03-5

  • 10g

  • 2,390.00CNY

  • Detail

24165-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name trityl thiohypochlorite

1.2 Other means of identification

Product number -
Other names Triphenylmethanesulfanyl Chloride

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:24165-03-5 SDS

24165-03-5Relevant articles and documents

Ciuffarin,Guaraldi

, p. 1745 (1969)

Catalytic asymmetric Pictet-Spengler reactions via sulfenyliminium ions

Wanner, Martin J.,Van Der Haas, Richard N. S.,De Cuba, Kimberly R.,Van Maarseveen, Jan H.,Hiemstra, Henk

, p. 7485 - 7487 (2008/09/17)

(Chemical Equation Presented) From cations to chiral products: β-Carbo-lines can be synthesized with good enantioselectivity by the title reaction catalyzed by a chiral binol-derived Bronsted acid (see scheme, BHT = 3,5-di(tert-butyl)-4-hydroxytoluene). T

The Synthesis of Substituted thio>acetic Acids

Woulfe, Steven R.,Miller, Marvin J.

, p. 3133 - 3139 (2007/10/02)

The synthesis of substituted thio>acetic acids (6, thiamazins) is described.Various substituted 3(S)-(acylamino)-2-azetidinones were sulfenylated with tert-butyl (phtalimidothio)acetate.Deprotection of the tert-butyl ester with trifluoroacetic acid provided the title compounds.In sharp contrast to their oxygen analogues (oxamazins), the thiamazins were devoid of biological activity.

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