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2,3,6-TRICHLOROPHENYLACETONITRILE, also known as TCPAN, is a chemical compound with the molecular formula C8H4Cl2N. It is a white solid that is insoluble in water and is primarily used as an intermediate in the synthesis of other organic compounds.

3215-65-4

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3215-65-4 Usage

Uses

Used in Agrochemical Industry:
2,3,6-TRICHLOROPHENYLACETONITRILE is used as a chemical intermediate for the production of agrochemicals, such as pesticides and herbicides, due to its versatile reactivity and ability to form various organic compounds.
Used in Pharmaceutical Industry:
2,3,6-TRICHLOROPHENYLACETONITRILE is used as a building block in the synthesis of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Dye Industry:
2,3,6-TRICHLOROPHENYLACETONITRILE is used as a chemical intermediate in the production of dyes, enabling the creation of a wide range of colorants for various applications.
Used in Organic Synthesis:
2,3,6-TRICHLOROPHENYLACETONITRILE is used as a versatile reagent in organic synthesis, allowing for the formation of various organic compounds for research and industrial purposes.
Note: It is important to handle and store 2,3,6-TRICHLOROPHENYLACETONITRILE with proper safety precautions, as it is considered a hazardous chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 3215-65-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,1 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3215-65:
(6*3)+(5*2)+(4*1)+(3*5)+(2*6)+(1*5)=64
64 % 10 = 4
So 3215-65-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H4Cl3N/c9-6-1-2-7(10)8(11)5(6)3-4-12/h1-2H,3H2

3215-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,3,6-trichlorophenyl)acetonitrile

1.2 Other means of identification

Product number -
Other names 2,3,6-Trichlorobenzyl cyanide

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:3215-65-4 SDS

3215-65-4Relevant academic research and scientific papers

FLUORINATED PHENYLACETIC ACID DERIVATIVES IN A WEED CONTROL METHOD

-

, (2021/05/21)

The present invention relates to the use of a compound of Formula (I), wherein R1, R2 and n are as defined herein as a herbicide. The invention further relates to agrochemically acceptable salts, to herbicidal compositions which comprise a compound of Formula (I) and to the use of compounds of Formula (I) for controlling weeds, in particular in crops of useful plants.

METABOLISM OF CHLOROPHENYLALANINES IN CROP AND WEED PLANTS IN RELATION TO THE FORMATION OF POTENTIAL HERBICIDAL END PRODUCTS

Taylor, David C.,Wightman, Frank,Kazakoff, Clem W.

, p. 51 - 72 (2007/10/02)

Metabolism of 12 synthetic D,L-chlorophenylalanines has been examined in several crop and weed plants.Twenty-five gram samples of excised shoots or leaves of bushbean, soybean, corn, pigweed, lambsquarters, and giant foxtail were allowed to metabolize 10-4 M solutions of the D,L-chlorophenylalanines for 24 hr in continuous light.The plant samples were then extracted in 80percent methanol and the soluble acidic metabolites fractionated into ether.Each ether concentrate was partially purified by fractional elution from a PrepSep C18 coloumn and then analysed by HPLC.Collected fractions were esterified with pentafluorobenzylbromide and examined by GC-MS to demonstrate the presence of PFB-esters of chlorophenylacetic, chlorobenzoic and/or chlorocinnamic acids.Since certain of these metabolites are known to be potent plant growth-regulators and herbicides, the results are discussed in relation to the potantial herbicidal action of certain chlorophenylalanines by the mechanism of 'lethal synthesis'.Key Word Index - Phaseolus vulgaris; Glycine max.; Leguminosae; Zea mays; Amaranthus retroflexus; Chenopodium album; Setaria faberii; metabolism; D,L-chlorophenylalanines; chlorophenylacetic acids; chlorobenzoic acids; chlorocinnamic acids; growth regulators.

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