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27328-86-5

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27328-86-5 Usage

Uses

3-(Trifluoromethyl)benzoylacetonitrile is used as a pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 27328-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,2 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27328-86:
(7*2)+(6*7)+(5*3)+(4*2)+(3*8)+(2*8)+(1*6)=125
125 % 10 = 5
So 27328-86-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H6F3NO/c11-10(12,13)8-3-1-2-7(6-8)9(15)4-5-14/h1-3,6H,4H2

27328-86-5 Well-known Company Product Price

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  • Alfa Aesar

  • (A15564)  3-(Trifluoromethyl)benzoylacetonitrile, 97%   

  • 27328-86-5

  • 1g

  • 807.0CNY

  • Detail
  • Alfa Aesar

  • (A15564)  3-(Trifluoromethyl)benzoylacetonitrile, 97%   

  • 27328-86-5

  • 5g

  • 2102.0CNY

  • Detail
  • Alfa Aesar

  • (A15564)  3-(Trifluoromethyl)benzoylacetonitrile, 97%   

  • 27328-86-5

  • 25g

  • 8836.0CNY

  • Detail

27328-86-5SDS

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 3-oxo-3-[3-(trifluoromethyl)phenyl]propanenitrile

1.2 Other means of identification

Product number -
Other names 3-Oxo-3-(3-(trifluoromethyl)phenyl)propanenitrile

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:27328-86-5 SDS

27328-86-5Relevant articles and documents

SPIROUREA DERIVATIVES

-

Page/Page column 94, (2021/11/06)

The invention relates to compounds of Formula (I) wherein X1, X2, X3, Y, R1, R2A, R2B, R3, and R4 are as described in the description; to their preparation, to pharmaceutically acceptable salts thereof, to pharmaceutical compositions containing one or more compounds of Formula (I), and to the use of such compounds as medicaments, especially as Kv7 openers.

Palladium-Catalyzed Carbonylative α-Arylation of tert -Butyl Cyanoacetate with (Hetero)aryl Bromides

Jensen, Mikkel T.,Juhl, Martin,Nielsen, Dennis U.,Jacobsen, Mikkel F.,Lindhardt, Anders T.,Skrydstrup, Troels

, p. 1358 - 1366 (2016/03/01)

A three-component coupling protocol has been developed for the generation of 3-oxo-3-(hetero)arylpropanenitriles via a carbonylative palladium-catalyzed α-arylation of tert-butyl 2-cyanoacetates with (hetero)aryl bromides followed by an acid-mediated decarboxylation step. Through the combination of only a stoichiometric loading of carbon monoxide and mild basic reaction conditions such as MgCl2 and dicyclohexylmethylamine for the deprotonation step, an excellent functional group tolerance was ensured for the methodology. Through the use of 13C-labeled carbon monoxide generated from 13COgen, the corresponding 13C-isotopically labeled β-ketonitriles were obtained, and these products could subsequently be converted into cyanoalkynes and 3-cyanobenzofurans with site specific 13C-isotope labeling. (Chemical Equation Presented).

Fungicidal cyclic amides

-

, (2008/06/13)

PCT No. PCT/US96/06534 Sec. 371 Date Nov. 13, 1997 Sec. 102(e) Date Nov. 13, 1997 PCT Filed May 8, 1996 PCT Pub. No. WO96/36616 PCT Pub. Date Nov. 21, 1996Compounds of Formula (I), and their N-oxides and agriculturally suitable salts are disclosed which are useful as fungicides, wherein E is 1,2-phenylene optionally substituted with one of R3, R4, or both R3 and R4; A is O; S; N; NR5; or CR14; G is C or N; provided that when G is C, then A is O, S or NR5 and the floating double bond is attached to G; and when G is N, then A is N or CR14 and the floating double bond is attached to A; W is O; S; NH; N(C1-C6 alkyl); or NO(C1-C6 alkyl); X is OR1; S(O)mR1; or halogen; R1 is C1-C6 alkyl; C1-C6 haloalkyl; C2-C6 alkenyl; C2-C6 haloalkenyl; C2-C6 alkynyl; C2-C6 haloalkynyl; C3-C6 cycloalkyl; C2-C4 alkylcarbonyl; or C2-C4 alkoxycarbonyl; R2 is H; C1-C6 alkyl; C1-C6 haloalkyl; C2-C6 alkenyl: C2-C6 haloalkenyl; C2-C6 alkynyl; C2-C6 haloalkenyl; C3-C6 cycloalkyl; C2-C4 alkylcarbonyl: C2-alkoxycarbonyl; hydroxy; C1-C2 alkoxy; or acetyloxy; and Y, Z, R3, R4, R5, R14 and m are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula (I) and a method for controlling plant diseases caused by fungal plant pathogens which involves applying an effective amount of a compound of Formula (I).

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