116272-78-7 Usage
General Description
2-Chloro-6-fluoro-omega-nitrostyrene is a chemical compound with the molecular formula C8H5ClFNO2. It is a yellow solid that is insoluble in water, but soluble in organic solvents. 2-CHLORO-6-FLUORO-OMEGA-NITROSTYRENE is used in the synthesis of pharmaceuticals and other organic compounds. It has potential applications in the production of dyes, pigments, and agrochemicals. Additionally, it can be used as a precursor in the manufacture of specialty chemicals. Due to its properties and potential uses, 2-chloro-6-fluoro-omega-nitrostyrene is a valuable compound in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 116272-78-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,7 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 116272-78:
(8*1)+(7*1)+(6*6)+(5*2)+(4*7)+(3*2)+(2*7)+(1*8)=117
117 % 10 = 7
So 116272-78-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H5ClFNO2/c9-7-2-1-3-8(10)6(7)4-5-11(12)13/h1-5H/b5-4+
116272-78-7Relevant articles and documents
Geometrically Selective Denitrative Trifluoromethylthiolation of β-Nitrostyrenes with AgSCF3for (E)-Vinyl Trifluoromethyl Thioethers
Fang, Ge,Hong, Jianquan,Huang, Shuai,Jiang, Chao,Liu, Yang,Zhang, Wei,Zheng, Changge
supporting information, (2020/07/03)
An efficient copper(II)-promoted denitrative trifluoromethylthiolation under mild reaction conditions has been developed for vinyl trifluoromethyl thioethers to construct Cvinyl-SCF3 bonds with stable AgSCF3 as a source of the trifluoromethylthio. This reaction system tolerates a broad range of functional groups to commendably achieve a high product yield and excellent stereoselectivity of E/Z.
Gel entrapped base catalysed (GEBC) Henry reaction: Synthesis of conjugated nitroalkenes
Bandgar,Uppalla
, p. 2071 - 2075 (2007/10/03)
A new, simple and practical procedure for direct transformation of aldehydes or ketones and nitromethane into conjugated nitroalkenes by using novel gel entrapped base catalyst (GEBC) has been described.
