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74114-75-3

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74114-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74114-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,1 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74114-75:
(7*7)+(6*4)+(5*1)+(4*1)+(3*4)+(2*7)+(1*5)=113
113 % 10 = 3
So 74114-75-3 is a valid CAS Registry Number.

74114-75-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzene sulfonyl-N'-carbo-tert-butoxy hydrazine

1.2 Other means of identification

Product number -
Other names -

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:74114-75-3 SDS

74114-75-3Downstream Products

74114-75-3Relevant articles and documents

An efficient synthesis of sulfonylhydrazides and sulfonylsemicarbazides by utilizing alumina as a catalyst

Safaei-Ghomi, Javad

, p. 1561 - 1563 (2007)

Sulfonyl hydrazides and sulfonyl semicarbazides are readily prepared by the reacting of hydrazine derivatives with sulfonyl chlorides in the presence of basic alumina under solvent-free conditions. Reaction of a sulfonyl chloride with t-butylcarbazate, followed by hydrolysis provides the corresponding sulfonyl hydrazides in higher yield and shorter time than previously reported.

Sulfonyl carbazates as blowing agents

-

, (2008/06/13)

Sulfonyl carbazates containing at least one group of: wherein the oxygen and the sulphur atoms attach to various organic groups are useful as high temperature blowing agents for gas-expandable polymers. Additionally, novel polyfunctional and secondary

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