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2-(4-chlorophenyl)-1,1,1-trifluoro-4-phenylbut-3-yn-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1304776-91-7

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1304776-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1304776-91-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,4,7,7 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1304776-91:
(9*1)+(8*3)+(7*0)+(6*4)+(5*7)+(4*7)+(3*6)+(2*9)+(1*1)=157
157 % 10 = 7
So 1304776-91-7 is a valid CAS Registry Number.

1304776-91-7Downstream Products

1304776-91-7Relevant academic research and scientific papers

Enantioselective Alkynylation of Trifluoromethyl Ketones Catalyzed by Cation-Binding Salen Nickel Complexes

Park, Dongseong,Jette, Carina I.,Kim, Jiyun,Jung, Woo-Ok,Lee, Yongmin,Park, Jongwoo,Kang, Seungyoon,Han, Min Su,Stoltz, Brian M.,Hong, Sukwon

supporting information, p. 775 - 779 (2019/12/24)

Cation-binding salen nickel catalysts were developed for the enantioselective alkynylation of trifluoromethyl ketones in high yield (up to 99 %) and high enantioselectivity (up to 97 % ee). The reaction proceeds with substoichiometric quantities of base (

Enantioselective alkynylation of trifluoromethyl ketones catalyzed by chiral Schiff bases

Dhayalan, Vasudevan,Murakami, Ryo,Hayashi, Masahiko

, p. 7505 - 7508 (2013/08/23)

Enantioselective alkynylation of trifluoromethyl ketones catalyzed by chiral Schiff bases in the presence of Me2Zn afforded the corresponding trifluoroalkynyl alcohols in up to 66 % ee.

Catalytic enantioselective alkynylation of trifluoromethyl ketones: Pronounced metal fluoride effects and implications of zinc-to-titanium transmetallation

Zhang, Guang-Wu,Meng, Wei,Ma, Hai,Nie, Jing,Zhang, Wen-Qin,Ma, Jun-An

supporting information; experimental part, p. 3538 - 3542 (2011/05/03)

Lost in transmetalation: The titanium(IV)-catalyzed title reaction, utilizing chiral cinchona alkaloids as ligands (L1 and L2), was developed for the synthesis of both enantiomers of trifluoromethylated propargylic tertiary alcohols in high yield and enan

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