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trans-2,2-Difluoro-3-phenylcyclopropan-1-carbonsaeure-methylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82045-10-1

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82045-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82045-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,4 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82045-10:
(7*8)+(6*2)+(5*0)+(4*4)+(3*5)+(2*1)+(1*0)=101
101 % 10 = 1
So 82045-10-1 is a valid CAS Registry Number.

82045-10-1Downstream Products

82045-10-1Relevant academic research and scientific papers

Fluoro Analoga of Cycloheptadiene Pheromones of Marine Brown Algae: Exceptionally Facile -Sigmatropic Rearrangement of a trans-Di(alkyl)-Substituted Geminal Difluorocyclopropane

Erbes, Petra,Boland, Wilhelm

, p. 766 - 772 (1992)

The 3,3-difluorocyclopropane-1,2-dicarbonyl compounds 9a and 9b are obtained by addition of difluorocarbene to methyl cinnamate or trans-stilbene followed by oxidative degradation of the phenyl rings(s) (Scheme 2).Compound 9b is a versatile building block

Transition Metal-free gem-difluorocyclopropanation of Alkenes with CF3SiMe3?NaI System: a Recipe for Electron-deficient Substrates

Nosik, Pavel S.,Ryabukhin, Sergey V.,Grygorenko, Oleksandr O.,Volochnyuk, Dmitriy M.

, p. 4104 - 4114 (2018/10/02)

Reaction of various electron-deficient alkenes, as well as functionalized styrene derivatives with CF3SiMe3?NaI system is studied. Relative reactivity of the substrates is established. It is shown that many α,β-unsaturated esters can

Studies on Organic Fluorine Compounds. 38. Ring-Opening Reactions of gem-Difluorocyclopropyl Ketones with Nucleophiles

Kobayashi, Yoshiro,Taguchi, Takeo,Morikawa, Tsutomu,Takase, Toyohiko,Takanashi, Hiroshi

, p. 3232 - 3236 (2007/10/02)

Syntheses of gem-difluorocyclopropyl ketones (3a-d) and their reactions with nucleophiles are described.Ring-opening reaction of 3a,c,d having a hydrogen substituent at C1 adjacent to the carbonyl group with a methanolate anion gave carboxylic acid derivatives derived from C1-C2 bond scission (between the carbon atom with an acyl group and the carbon atom with fluorine substituents).On the other hand, reaction of 3a-c with a thiolate anion resulted in the C1-C3 bond cleavage (carbon-carbon bond opposite to the difluoromethylene group).

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