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2-(3-Chlorophenyl)-3-phenyl oxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52881-67-1

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52881-67-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52881-67-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,8 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52881-67:
(7*5)+(6*2)+(5*8)+(4*8)+(3*1)+(2*6)+(1*7)=141
141 % 10 = 1
So 52881-67-1 is a valid CAS Registry Number.

52881-67-1Relevant academic research and scientific papers

Chiral Macrocyclic Organocatalysts for Kinetic Resolution of Disubstituted Epoxides with Carbon Dioxide

Ema, Tadashi,Yokoyama, Maki,Watanabe, Sagiri,Sasaki, Sota,Ota, Hiromi,Takaishi, Kazuto

supporting information, p. 4070 - 4073 (2017/08/15)

Among chiral macrocycles 1 synthesized, 1m with the 3,5-bis(trifluoromethyl)phenylethynyl group was the best organocatalyst for the enantioselective synthesis of cyclic carbonates from disubstituted or monosubstituted epoxides and CO2. The X-ray crystal structure of 1m revealed a well-defined chiral cavity with multiple hydrogen-bonding sites that is suitable for the enantioselective activation of epoxides. A catalytic cycle proposed was supported by DFT calculations.

A new synthesis of trans-2,3-diaryloxiranes and 2-(1 H -benzo[ d ][1,2,3]-triazol-1-yl)-1-arylethanols via the reactions of 1-benzyl-3- methylbenzo-triazolium ylide with aryl aldehydes

Xiao, Xiaohui,Lin, Daqin,Tong, Shuitian,Mo, Hailan

experimental part, p. 2823 - 2826 (2011/12/21)

1-Benzyl-3-methylbenzotriazolium ylide was formed by the reaction of 1-benzyl-3-methylbenzotriazolium iodide with t-BuOK. Subsequently it reacted with various aryl aldehydes to give the corresponding trans-2,3-diaryloxiranes and 2-(1H-benzo-[d][1,2,3]triazol-1-yl)-1-arylethanols in moderate to high yields. Georg Thieme Verlag Stuttgart · New York.

Process for the preparation of an oxirane, azirdine or cyclopropane

-

, (2008/06/13)

A process for the preparation of an oxirane, aziridine or cyclopropane of formula (I) wherein, X is oxygen, NR4 or CHR5 ; R1 is hydrogen, alkyl, aryl, heteroaromatic, heterocyclic or cycloalkyl; R2 is hydrogen, alkyl, aryl, heteroaromatic, CO2 R8, CHR14 NHR13, heterocyclic or cycloalkyl; or R1 and R2 join together to form a cycloalkyl ring; R3 is hydrogen, alkyl, aryl, heteroaromatic, CO2 R8, R83 Sn, CONR8 R9 or trimethylsilyl; R4 and R5 are, independently, alkyl, cycloalkyl, aryl, heteroaromatic, SO2 R8, SO3 R8, COR8, CO2 R8, CONR8 R9 or CN, or R4 can also be P(O)(aryl)2 ; R8 and R9 are independently alkyl, aryl or arylalkyl; R13 and R14 are independently hydrogen, alkyl or aryl; the process comprising reacting a mixture of a compound of formula (II), wherein R1, R2 and X are as defined above, and a sulphide of formula SR6 R7, wherein R6 and R7 are independently alkyl, aryl or heteroaomatic, or R6 and R7 join together to form a cycloalkyl ring which optionally includes an additional heteroatom, with either (i) a metallocarbon obtainable by reacting an alkylmetal with a methane derivative of formula CHR3 X'X", wherein R3 is as defined above, and X' and X" are independently, a leaving group, or (ii) a metallocarbon obtainable by reacting a compound of formula (III), (wherein R3 may not be hydrogen) with a suitable organometallic or inorganic reagent.

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