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(R)-4-(2-fluorophenyl)-4-hydroxybutan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1192275-80-1

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1192275-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1192275-80-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,2,7 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1192275-80:
(9*1)+(8*1)+(7*9)+(6*2)+(5*2)+(4*7)+(3*5)+(2*8)+(1*0)=161
161 % 10 = 1
So 1192275-80-1 is a valid CAS Registry Number.

1192275-80-1Downstream Products

1192275-80-1Relevant academic research and scientific papers

Telaprevir fragments as organocatalysts in asymmetric direct aldol reactions of aldehydes

Weng, Chen Chen,Xu, Xinliang,Xiong, Xiao Xia,Lu, Xiu Lian,Zhou, Yi Feng

, p. 2447 - 2452 (2013)

We have demonstrated that the fragments of Telaprevir can act as organocatalysts for asymmetric aldol reactions between aromatic aldehydes and acetone under mild conditions. The reaction conditions have been optimized in terms of the catalyst nature, choi

Prolinamide-Derived Ionic-Liquid-Supported Organocatalyst for Asymmetric Mono- and Bis-Aldol Reactions in the Presence of Water

Kucherenko, Aleksander S.,Gerasimchuk, Vasiliy V.,Lisnyak, Vladislav G.,Nelyubina, Yulia V.,Zlotin, Sergei G.

, p. 5649 - 5654 (2015/09/01)

A novel recyclable prolinamide-derived ionic-liquid-supported organocatalyst of asymmetric cross-aldol reactions in aqueous medium has been developed. In its presence, aromatic aldehydes react with cyclic or linear ketones to afford chiral aldol adducts i

Proline-threonine dipeptide as an organocatalyst for the direct asymmetric aldol reaction

Chandrasekhar, Srivari,Johny, Kancharla,Reddy, Chada Raji

experimental part, p. 1742 - 1745 (2009/12/26)

A new proline-threonine (H-Pro-Thr-OH) dipeptide has been demonstrated as an efficient organocatalyst for a direct asymmetric aldol reaction. It was found that this new peptide-based catalyst efficiently catalyzed the reaction between an aldehyde and acetone to provide β-hydroxy ketones in good yields with good enantioselectivities.

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