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2-fluoro-1-acetoxy-1,1-diphenylethane is an organic compound characterized by its molecular formula C16H15FO2. 2-fluoro-1-acetoxy-1,1-diphenylethane features a fluorinated ethyl group (-CH2F), an acetoxy group (-OAc), and two phenyl rings (C6H5) bonded to the central carbon atoms. The acetoxy group is attached to the carbon adjacent to the fluorine, while the phenyl rings are connected to the other carbon. This structure endows the molecule with unique chemical properties, making it a potential candidate for various applications in organic synthesis, pharmaceuticals, and materials science. The compound's synthesis and reactivity are of interest to chemists due to its fluorinated and acetoxylated nature, which can influence its electronic and steric properties, as well as its potential for further functionalization.

960-02-1

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960-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 960-02-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 960-02:
(5*9)+(4*6)+(3*0)+(2*0)+(1*2)=71
71 % 10 = 1
So 960-02-1 is a valid CAS Registry Number.

960-02-1Downstream Products

960-02-1Relevant academic research and scientific papers

A 2 - fluoro - 1, 1 - phenyl ethyl acetate synthesis method

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Paragraph 0018; 0019; 0032; 0044, (2018/10/11)

The invention discloses a method for synthesizing 2 - fluoro - 1, 1 - phenyl ethyl acetate method, in order to 1, 1 - diphenyl ethylene as raw materials, glacial acetic acid as nucleophiles, fluorine Selectfluor reagent, molecule to fluorinated esterifica

Catalyst-free fluorinative alkoxylation of alkenes

Hou, Hong,Li, Hengxue,Xu, Yue,Tang, Daliang,Han, Ying,Yan, Chaoguo,Chen, Xiaoyun,Zhu, Shaoqun

supporting information, p. 6577 - 6583 (2018/10/04)

The fluorinative alkoxylation of simple alkenes under catalyst-free conditions was achieved. Various substituted olefins, including terminal and internal alkenes, and oxygen-containing nucleophiles were compatible with the standard conditions, and gave a

1-Fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) as a new, effective reagent for selective fluorofunctionalisation of alkenes under mild reaction conditions

Stavber, Stojan

, p. 6769 - 6772 (2007/10/02)

1-Fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) Accufluor NFTh) is confirmed as a highly effective reagent for introducing a fluorine atom into organic molecules across a phenyl-substituted carbon-carbon double bond. Quantitativ

FLUORINATION WITH CAESIUM FLUOROXYSULPHATE. ROOM TEMPERATURE FLUORINATION OF PHENYL SUBSTITUTED OLEFINS

Stavber, Stojan,Zupan, Marko

, p. 5035 - 5044 (2007/10/02)

Room -temperature fluorination of 1,1-diphenylethene with caesium fluoroxysulphate in methylene chloride resulted in an addition elimination process, thus yielding 1,1-diphenyl-2-fluoroethene, while in the presence of nucleophile containing species, i.e.,

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