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83029-57-6

83029-57-6

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83029-57-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83029-57-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,2 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83029-57:
(7*8)+(6*3)+(5*0)+(4*2)+(3*9)+(2*5)+(1*7)=126
126 % 10 = 6
So 83029-57-6 is a valid CAS Registry Number.

83029-57-6SDS

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-(2-[2-hydroxy-3-phenoxypropyl]aminoethyl)-isobutyramide

1.2 Other means of identification

Product number -
Other names 1-phenoxy-3-β-isobutyramidoethylamino-2-propanol

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:83029-57-6 SDS

83029-57-6Downstream Products

83029-57-6Relevant articles and documents

Method of treatment of obesity

-

, (2008/06/13)

A method of treatment of obesity or diabetes mellitus in a warm-blooded animal requiring such treatment which comprises administering to said animal an effective amount of the compound N-(2-[2-hydroxy-3-phenoxypropyl]aminoethyl)-isobutyramide in racemic (R,S) or levorotatory optically active (S) form, or of a pharmaceutically acceptable acid-addition salt thereof.

β-Adrenergic Blocking Agents. 22. 1-Phenoxy-3-amino>-2-propanols

Large, M.S.,Smith, L.H.

, p. 1286 - 1292 (2007/10/02)

The synthesis of a series of 1-phenoxy-3-amino>-2-propanols is described.Many of the compounds are more potent than propanolol as β blockers, while having cardioselectivity comparable to that of practolol, when given intravenous

ALKANOLAMINE DERIVATIVES

-

, (2008/06/13)

Novel 1-aryloxy-3-amidoalkylamino-2-propanol derivatives, processes for their manufacture, pharmaceutical compositions containing them and methods of using them in the treatment of heart diseases. The compounds possess β-adrenergic blocking activity and s

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