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60548-64-3

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60548-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60548-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,4 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60548-64:
(7*6)+(6*0)+(5*5)+(4*4)+(3*8)+(2*6)+(1*4)=123
123 % 10 = 3
So 60548-64-3 is a valid CAS Registry Number.

60548-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4-dimethyl-1-sulfamoyloxypentan-3-yl) sulfamate

1.2 Other means of identification

Product number -
Other names Sulfamic acid,2-methyl-2-propyltrimethylene ester

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:60548-64-3 SDS

60548-64-3Downstream Products

60548-64-3Relevant articles and documents

Synthesis and Evaluation of the Male Antifertility Properties of a Series of N-Unsubstituted Sulfamates

Hirsch, Allen F.,Kasulanis, Charles,Kraft, Larry,Mallory, Robert A.,Powell, Gregory,Wong, Benny

, p. 901 - 903 (2007/10/02)

A series of six aliphatic and one carbocyclic N-unsubstituted sulfamates have been synthesized and evaluated as potential male antifertility agents.Three of the aliphatic sulfamates 1,2-ethanediyl sulfamate (1), 1,3-propanediyl sulfamate (2), and 1,4-butanediyl sulfamate (3), when administered orally to male rats caused a decrease in the number of pregnant females and/or implantation coupled with increased embryonic and fetal resorption.The compounds were prepared by treating the appropriate glycol salt with sulfamoyl chloride or by the cleavage of a tert-butylsulfamate with trifluoroacetic acid.

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