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6-OXO-6-(4-TRIFLUOROMETHYLPHENYL)HEXANENITRILE is a complex organic chemical compound with the molecular formula C13H14F3NO. It is characterized by a hexanenitrile backbone, which features a nitrile group (C≡N) at one end and a 6-oxo (carbonyl) group at the other. The molecule also includes a 4-trifluoromethylphenyl group, which is a phenyl ring (C6H5) with three fluorine atoms attached to the 4-position. 6-OXO-6-(4-TRIFLUOROMETHYLPHENYL)HEXANENITRILE is likely to be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and functional groups. It is important to handle such chemicals with care, as they can be reactive and may have specific safety considerations.

61718-88-5

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61718-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61718-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,1 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61718-88:
(7*6)+(6*1)+(5*7)+(4*1)+(3*8)+(2*8)+(1*8)=135
135 % 10 = 5
So 61718-88-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H12F3NO/c14-13(15,16)11-7-5-10(6-8-11)12(18)4-2-1-3-9-17/h5-8H,1-4H2

61718-88-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-oxo-6-[4-(trifluoromethyl)phenyl]hexanenitrile

1.2 Other means of identification

Product number -
Other names 6-OXO-6-(4-TRIFLUOROMETHYLPHENYL)HEXANENITRILE

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 -
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More Details:61718-88-5 SDS

61718-88-5Relevant academic research and scientific papers

Visible light-induced palladium-catalyzed ring opening β-H elimination and addition of cyclobutanone oxime esters

Xing, Wei-Long,Shang, Rui,Wang, Guang-Zu,Fu, Yao

supporting information, p. 14291 - 14294 (2019/12/02)

A palladium catalyst under visible light irradiation activates cyclobutanone oxime ester through single electron transfer to induce radical ring opening to generate hybrid cyanoalkyl Pd(i) radical species. Hybrid cyanoalkyl Pd(i) radical species can undergo either β-H elimination to deliver (E)-4-arylbut-3-enenitrile or undergo radical addition with silyl enol ether and enamide to generate δ-cyano ketones. A dual ligand system composed of two phosphine ligands is essential for the high reactivity.

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