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3,5-DICHLORO-2-HYDROXYBENZYLAMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38060-64-9

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38060-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38060-64-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,6 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38060-64:
(7*3)+(6*8)+(5*0)+(4*6)+(3*0)+(2*6)+(1*4)=109
109 % 10 = 9
So 38060-64-9 is a valid CAS Registry Number.

38060-64-9SDS

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-(Aminomethyl)-4,6-dichlorophenol

1.2 Other means of identification

Product number -
Other names 2-hydroxy-3,5-dichloro-benzylamine

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:38060-64-9 SDS

38060-64-9Relevant academic research and scientific papers

SUBSTITUTED PYRIMIDINES

-

Page/Page column 26, (2008/06/13)

The invention relates to novel substituted pyrimidines of formula (I), in which R1, R2, R3, R4, Q, X and n have the meanings as cited in the description. The invention also relates to a method and intermediate products for producing these pyrimidines, and to the use thereof as plant control agents, particularly as herbicides.

2-(Aminomethyl)phenols, a new class of saluretic agents. I. Effect of nuclear substitution

Stokker,Deana,deSolms,Schultz,Smith,Cragoe Jr.,Baer,Ludden,Russo,Scriabine,Sweet,Watson

, p. 1414 - 1427 (2007/10/02)

A series of 2-(aminomethyl)phenols was synthesized and tested in rats and dogs for saluretic and diuretic activity. A number of these compounds exhibit a high order of activity on iv or po administration. The most active compounds belong to a subseries of 4-alkyl-6-halo derivatives of which 2,2(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenyl, is the most active. Compound 2 also possesses significant antihypertensive activity, an adjunctive pharmacological parameter which distinguishes 2 from the other compounds prepared in this series. In addition, 2 displays both topical saluretic and antiinflammatory activities.

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