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21244-78-0

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21244-78-0 Usage

Type of compound

Nitrile

Constituents

Two chlorine atoms, phenoxy ring

Uses

Herbicide and pesticide in agricultural applications to control unwanted vegetation

Mode of action

Inhibits growth of target plants by disrupting hormone balance and interfering with cell division

Toxicity

Toxic to aquatic life, potential harm to human health if not handled and used properly

Environmental concerns

Persistent in the environment, long-term impact on ecosystems a concern

Check Digit Verification of cas no

The CAS Registry Mumber 21244-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,4 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21244-78:
(7*2)+(6*1)+(5*2)+(4*4)+(3*4)+(2*7)+(1*8)=80
80 % 10 = 0
So 21244-78-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H5Cl2NO/c9-6-2-1-3-7(10)8(6)12-5-4-11/h1-3H,5H2

21244-78-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,6-DICHLOROPHENOXY)ACETONITRILE

1.2 Other means of identification

Product number -
Other names HMS565H14

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:21244-78-0 SDS

21244-78-0Relevant articles and documents

Synthesis of eudistomin C and E: Improved preparation of the indole unit

Yamagishi, Hiroaki,Matsumoto, Koji,Iwasaki, Kotaro,Miyazaki, Tohru,Yokoshima, Satoshi,Tokuyama, Hidetoshi,Fukuyama, Tohru

supporting information; experimental part, p. 2369 - 2372 (2009/05/26)

(Chemical Equation Presented) An improved synthesis of the indole unit, a key intermediate for eudistomin C, was established utilizing Makosza's indole synthesis. A concise total synthesis of eudistomin E was achieved on the basis of the improved synthesi

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