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(S)-3-(4,4'-dimethyl)diphenylaminopropene oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

950171-33-2

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950171-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 950171-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,1,7 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 950171-33:
(8*9)+(7*5)+(6*0)+(5*1)+(4*7)+(3*1)+(2*3)+(1*3)=152
152 % 10 = 2
So 950171-33-2 is a valid CAS Registry Number.

950171-33-2Downstream Products

950171-33-2Relevant academic research and scientific papers

Anionic polymerization of optically active propene oxides bearing substituted N,N-diphenylamino moiety

Zhang, Jin,Zhao, Chun-Hui,Yang, Li-Wen,Yang, Nian-Fa

, p. 250 - 252 (2015)

A series of novel chiral propene oxides bearing substituted N,N-diphenylamino moiety were synthesized and anionically polymerized. Most of propene oxides gave polymers possessing high specific rotation and intensive circular dichroism (CD) signals, which

Enantioselective incorporation of carbon dioxide into epoxides catalyzed by optically active cobalt(II) complexes

Yamada, Wataru,Kitaichi, Yasunori,Tanaka, Hirotaka,Kojima, Tomohide,Sato, Mitsuo,Ikeno, Taketo,Yamada, Tohru

experimental part, p. 1391 - 1401 (2009/06/20)

The enantioselective chemical fixation of CO2 into an epoxide was developed using an optically active ketoimi-natocobalt(II) complex as a chiral Lewis acid. In the presence of a catalytic amount of the cobalt complex and amine base, enantioselective CO2 fixation with an epoxide proceeded with kinetic resolution to afford the corresponding carbonate along with unreacted epoxide, both of which were optically active. To improve their enantioselectivities, the ligand structures of the cobalt complexes and amine bases were examined. Thus, the optimized catalytic system was successfully applied to various epoxides to obtain the corresponding optically active cyclic carbonates and to recover epoxides with good-to-high enantioselectivities.

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