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13764-54-0

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13764-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13764-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,6 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13764-54:
(7*1)+(6*3)+(5*7)+(4*6)+(3*4)+(2*5)+(1*4)=110
110 % 10 = 0
So 13764-54-0 is a valid CAS Registry Number.

13764-54-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Isoproterenol Sulfate

1.2 Other means of identification

Product number -
Other names 1,2-Benzenediol,4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]-,(R)-,sulfate (2:1) (salt) (9CI)

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:13764-54-0 SDS

13764-54-0Relevant articles and documents

Method for preparing isoproterenol sulfate dihydrate

-

Paragraph 0021, (2017/09/01)

The invention relates to a method for preparing isoproterenol sulfate dihydrate. The method comprises the following steps: (1) preparation of 2-bromo-1-(3, 4-dihydroxy phenyl)-ethanone; (2) preparation of isoproterenol ketone hydrochloride; and (3) preparation of isoproterenol sulfate dihydrate. The method disclosed by the invention adopts a reaction system of bromoacetyl bromide and aluminium chloride instead of a reaction system of monochloro acetic acid and phosphorus oxychloride, so that the method has the advantages that the environmental protection cost is reduced; the reaction yield is increased; the industrial production is benefited; the reaction condition is mild; the catalyst quantity is little; and the process is simple. Compared with conventional synthetic processes, the method disclosed by the invention has obvious economic benefit and environmental benefit.

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