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17796-75-7

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17796-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17796-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,9 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17796-75:
(7*1)+(6*7)+(5*7)+(4*9)+(3*6)+(2*7)+(1*5)=157
157 % 10 = 7
So 17796-75-7 is a valid CAS Registry Number.

17796-75-7SDS

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 2-tert-butyl-3-sulfanylideneisoindol-1-one

1.2 Other means of identification

Product number -
Other names N-tert-butylsulfanyl-phthalimide

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:17796-75-7 SDS

17796-75-7Downstream Products

17796-75-7Relevant articles and documents

Desulfurization of Alkyl Phthalimido Disulfides

Rastetter, William H.,Spero, Denice M.,Adams, Julian,Harpp, David N.,Ash, David K.

, p. 2785 - 2787 (1982)

-

Preparation of sulfenyl pyrroles

Gillis, H. Martin,Greene, Lana,Thompson, Alison

experimental part, p. 112 - 116 (2009/06/18)

Sulfenyl groups are attracting interest as masking/protecting groups for pyrroles. A facile one-step synthesis of sulfenyl pyrroles, involving the reaction of pyrroles with N-(aryl- and alkylthio)phthalimides in the presence of MgBr2, is reported and the methodology extends to include sulfinyl pyrroles. The one-step procedure gives good yields and is more efficient and practical than current multistep protocols to sulfenyl pyrroles that involve thiocyanato pyrrolic intermediates. A convenient procedure for the synthesis of N-(aryl- and alkylthio)phthalimides is also reported. Georg Thieme Verlag Stuttgart.

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