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beta-oxo-alpha-[3-(trifluoromethyl)phenyl]benzenebutyronitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68084-26-4

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68084-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68084-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,8 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 68084-26:
(7*6)+(6*8)+(5*0)+(4*8)+(3*4)+(2*2)+(1*6)=144
144 % 10 = 4
So 68084-26-4 is a valid CAS Registry Number.

68084-26-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-oxo-4-phenyl-2-[3-(trifluoromethyl)phenyl]butanenitrile

1.2 Other means of identification

Product number -
Other names EINECS 268-435-0

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:68084-26-4 SDS

68084-26-4Relevant academic research and scientific papers

Synthesis method of 1-phenyl-3-(3-trifluoromethylphenyl)-2-acetone

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, (2021/11/21)

The invention belongs to the technical field of chemical intermediates, and particularly relates to a synthesis method of 1-phenyl-3-(3-trifluoromethylphenyl)-2-acetone. A compound A is used as a basic raw material, and 1-phenyl-3-(3-trifluoromethylphenyl)-2-acetone is obtained through Blanc chloromethylation, substitution reaction, Claisen ester condensation and hydrolysis reaction in sequence. The synthesis method of 1-phenyl-3-(3-trifluoromethylphenyl)-2-acetone is high in purity, high in yield and simple to operate.

Fufu grass alkone intermediate preparation method (by machine translation)

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Paragraph 0021-0023, (2017/09/02)

The invention discloses a method of preparing intermediates of fufu grass alkone, including: (1) to between three happens b nitrile and benzene acetyl chloride as the starting material, tertiary butyl alcohol sodium and organic solvent in the presence of the intermediate obtained by reaction of (3 - trifluoromethyl-phenyl) - benzyl carbonyl - b nitriles; (2) intermediate (3 - trifluoromethyl-phenyl) - benzyl carbonyl - acetonitrile and glacial acetic acid by the reaction of bromine fufu grass alkone intermediate 2 - phenyl - 3 - oxo - 4 - (3 - trifluoromethyl-phenyl) - 5 - amino - 2, 3 - dihydrofuran. Preparation method of this invention mild reaction, after treatment is simple, safety and environmental protection, especially few by-products, the product has high purity, and thus is suitable for industrial production. (by machine translation)

[...] method for the production of efficient herbicide (by machine translation)

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Paragraph 0023, (2016/10/10)

The invention discloses an efficient method of producing herbicide [...], to trifluoromethyl benzene b nitrile and benzene acetic acid ethyl ester as the main raw material, the claisen condensation, cyclization under in an acidic solvent, methylation three steps [...] the target product can be obtained. The present invention has higher safety, for reaction and purification conditions is relatively low, it is relatively easy to separate, and is not easy to generate discharge of waste acid, the solvent can be recycled, the production yield is higher. This method is more suitable for the industrial production of [...], [...] is more favorable for the wide application of efficient herbicide. (by machine translation)

Herbicidal 5-amino-3-oxo-4-(substituted-phenyl)-2,3-dihydrofuran and derivatives thereof

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, (2008/06/13)

5-Amino-3-oxo-4-(substituted-phenyl)-2,3-dihydrofuran and derivatives thereof. The compounds generally exhibit both pre-emergence and post-emergence phytotoxicity and are useful as herbicides and also at low dosages as plant growth regulating agents.

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