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(2S,3R)-2-Chloro-3-methoxy-1,3-diphenyl-propan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38680-14-7

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38680-14-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38680-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,8 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38680-14:
(7*3)+(6*8)+(5*6)+(4*8)+(3*0)+(2*1)+(1*4)=137
137 % 10 = 7
So 38680-14-7 is a valid CAS Registry Number.

38680-14-7Downstream Products

38680-14-7Relevant academic research and scientific papers

Catalytic asymmetric intra- and intermolecular haloetherification of enones: An efficient approach to (?)-Centrolobine

Zhou, Pengfei,Cai, Yunfei,Zhong, Xia,Luo, Weiwei,Kang, Tengfei,Li, Jun,Liu, Xiaohua,Lin, Lili,Feng, Xiaoming

, p. 7778 - 7783 (2016)

A catalytic asymmetric intra- and intermolecular haloetherification of electron-deficient alkenes (halogen = Cl, Br, I) has been realized by the use of chiral metal complexes of N,N′-dioxides. In the presence of a chiral Fe(III) complex, a series of tetrahydropyran derivatives were obtained in good yields (up to 99% yield) with a high level of enantioselectivities (up to 97% ee). Promoted by a chiral Ce(III) complex, chiral oxepane derivatives could be given in good results. Moreover, the intermolecular haloetherification of chalcones catalyzed by Sc(III) complex using MeOH as nucleophile is demonstrated. This methodology also can be successfully applied to the synthesis of (?)-Centrolobine. Meanwhile, a reasonable reaction mechanism was proposed.

The vicinal functionalization of olefins: A facile route to the direct synthesis of β-chlorohydrins and β-chloroethers

Swamy, Peraka,Kumar, Macharla Arun,Reddy, Marri Mahender,Naresh, Mameda,Srujana, Kodumuri,Narender, Nama

, p. 26288 - 26294 (2014/07/08)

An efficient and environmentally benign protocol for the synthesis of vicinal chlorohydroxy and chloromethoxy derivatives in a highly regioselective manner from olefins using NH4Cl as a chlorine source and oxone as an oxidant in aqueous acetone and methanol is demonstrated. This methodology offers an additive and metal chloride free approach and is endowed with simple reaction conditions, high yields a broad substrate scope and good functional group tolerance. Moreover, the aromatic substrates with a terminal double bond exhibited merely Markovnikov selectivity, while the internal alkenes show exclusive regiocontrol and low to moderate diastereoselectivity.

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