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13553-69-0

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13553-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13553-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,5 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13553-69:
(7*1)+(6*3)+(5*5)+(4*5)+(3*3)+(2*6)+(1*9)=100
100 % 10 = 0
So 13553-69-0 is a valid CAS Registry Number.

13553-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name S,S-diethyl-N-(toluene-4-sulfonyl)-sulfimide

1.2 Other means of identification

Product number -
Other names S.S-Diethyl-N-p-toluolsulfonylsulfilimin

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:13553-69-0 SDS

13553-69-0Relevant articles and documents

[FeIII(F20-tpp)Cl] Is an effective catalyst for nitrene transfer reactions and animation of saturated hydrocarbons with sulfonyl and aryl azides as nitrogen source under thermal and microwave-assisted conditions

Liu, Yungen,Che, Chi-Ming

experimental part, p. 10494 - 10501 (2010/10/21)

[FeIII(F20-tpp)Cl] (F20tpp = meso- tetrakis(pentafluorophenyl)porphyrinato dianion) is an effective catalyst for imido/nitrene insertion reactions using sulfonyl and aryl azides as nitrogen source. Under thermal conditions, aziridination of aryl and alkyl alkenes (16 examples, 60-95% yields), sulfimidation of sulfides (11 examples, 76-96% yields), allylic amidation/amination of α-methylstyrenes (15 examples, 68-83% yields), and amination of saturated C-H bonds including that of cycloalkanes and adamantane (eight examples, 64-80% yields) can be accomplished by using 2 mol % [FeIII(F20- tpp)Cl] as catalyst. Under microwave irradiation conditions, the reaction time of aziridination (four examples), allylic amination (five examples), sulfimidation (two examples), and amination of saturated C-H bonds (three examples) can be reduced by up to 16fold (24-48 versus 1.5-6 h) without significantly affecting the product yield and substrate conversion.

Hypervalent iodine in synthesis XXXII: A novel way for the synthesis of N-sulfonylsulfilimines from sulfides and sulfonamides using iodosobenzene diacetate

Ou, Wei,Chen, Zhen-Chu

, p. 4443 - 4449 (2007/10/03)

A number of N-sulfonylsulfilimines have been prepared through a novel way for the reaction of iodosobenzene diacetate with sulfides and sulfonamides under mild conditions.

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