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1-(3-difluoromethoxy-phenyl)-ethylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

926263-64-1

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926263-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 926263-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,6,2,6 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 926263-64:
(8*9)+(7*2)+(6*6)+(5*2)+(4*6)+(3*3)+(2*6)+(1*4)=181
181 % 10 = 1
So 926263-64-1 is a valid CAS Registry Number.

926263-64-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(Difluoromethoxy)phenyl]ethanamine

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:926263-64-1 SDS

926263-64-1Downstream Products

926263-64-1Relevant academic research and scientific papers

Synthesis of benzylaminopyrimidines and their fungicidal activities against wheat brown rust and barley powdery mildew

Yamanaka,Moritomo,Fujii,Tanaka,Fukuda,Nishimura

, p. 223 - 229 (2007/10/03)

Members of a new class of fungicide containing benzyl-aminopyrimidine as a core structure were synthesized and their fungicidal potencies against wheat brown rust, Puccinia recondita, and barley powdery mildew, Erysiphe graminis, were assessed. Among these fungicides, N-(fluoroalkoxy or fluorophenoxybenzyl)-4-pyrimidinamines showed notable preventive activities. The potency of the new pyrimidines was increased when a difluoromethoxy or tetrafluorophenoxy group was introduced at the 4- or 3-position of the phenyl moiety and a methyl or ethyl group was introduced at the benzyl position. Structure-activity relationships are discussed.

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