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34715-64-5

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34715-64-5 Usage

Preparation

Obtained by condensation of a-chloro-3,4-dihydroxy-acetophenone with tert-butylamine in dioxane at 60–80°. The amino ketone base which separated was treated with concentrated hydrochloric acid.

Check Digit Verification of cas no

The CAS Registry Mumber 34715-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,1 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34715-64:
(7*3)+(6*4)+(5*7)+(4*1)+(3*5)+(2*6)+(1*4)=115
115 % 10 = 5
So 34715-64-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO3.ClH/c1-12(2,3)13-7-11(16)8-4-5-9(14)10(15)6-8;/h4-6,13-15H,7H2,1-3H3;1H

34715-64-5SDS

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-(tert-butylamino)-1-(3,4-dihydroxyphenyl)ethanone,hydrochloride

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:34715-64-5 SDS

34715-64-5Relevant articles and documents

USE OF CATECHOLAMINES AND RELATED COMPOUNDS AS ANTI-ANGIOGENIC AGENTS

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Page/Page column 17, (2008/12/07)

A catecholamine or related compound of formula (I) having (S)-configuration at β-carbon and having a lipophilicity greater than (S)- noradrenalme, a physiologically tolerated salt thereof, a prodrug thereof, a physiologically functional derivative thereof or any mixture thereof is useful as an anti-angiogemc agent A catecholamine or related compound of formula (II) in which a β-hydroxy group has been modified is also anti-angiogemc

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