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Benzamide, N-(2-hydroxy-1,2-diphenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66166-17-4

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66166-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66166-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,6 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66166-17:
(7*6)+(6*6)+(5*1)+(4*6)+(3*6)+(2*1)+(1*7)=134
134 % 10 = 4
So 66166-17-4 is a valid CAS Registry Number.

66166-17-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-hydroxy-1,2-diphenylethyl)benzamide

1.2 Other means of identification

Product number -
Other names Benzamide,N-(2-hydroxy-1,2-diphenylethyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:66166-17-4 SDS

66166-17-4Relevant academic research and scientific papers

Asymmetric Transfer Hydrogenation: Dynamic Kinetic Resolution of α-Amino Ketones

Gediya, Shweta K.,Clarkson, Guy J.,Wills, Martin

, p. 11309 - 11330 (2020/10/12)

A series of α-amino ketones were reduced using asymmetric transfer hydrogenation (ATH) through a dynamic kinetic resolution (DKR). The protecting group was matched to the reducing agent, and following optimization, a series of substrates were investigated, giving products in high diastereoselectivity, over 99% ee in several cases and full conversion. The methodology was applied to the enantioselective synthesis of an MDM2-p53 inhibitor precursor.

Lewis Acid-Catalyzed Addition of Benzophenone Imine to Epoxides Enables the Selective Synthesis and Derivatization of Primary 1,2-Amino Alcohols

Leitch, David C.,Lim, John Jin

, p. 641 - 649 (2018/05/14)

Benzophenone imine was found to be an effective ammonia surrogate for the selective preparation of primary 1,2-amino alcohols from epoxides, including enantiopure epichlorohydrin, in the presence of catalytic Y(OTf)3. High-throughput screening of 48 Lewis acids quickly identified Y(OTf)3 as an effective mediator of the addition reaction under mild conditions. Following acidic hydrolysis, the primary amino alcohol salt is revealed and partitions into the aqueous solution, while the benzophenone byproduct is easily removed by simple extraction with ethyl acetate. These ammonium salts can be directly Boc-protected or further derivatized without isolation to form benzamides and sulfonamides under Schotten-Baumann-type conditions in up to 79% isolated yield over three steps. This methodology has been used to prepare key intermediates for the synthesis of PRMT5 inhibitors with high enantiopurity as well as numerous other amide and sulfonamide derivatives.

REACTIVITY OF N,N-DICHLOROURETHANES. XI. ADDITION OF N,N-DICHLOROURETHANES TO trans-STILBENE

Bal'on, Ya. G.,Moskaleva, R. N.

, p. 2227 - 2232 (2007/10/02)

N,N-Dichlorourethanes add readily to trans-stilbene with the formation of alkyl N-chloro-N-(2-chloro-1,2-diphenylethyl)carbamates, which give alkyl N-(2-chloro-1,2-diphenylethyl)carbamates when treated with an aqueous solution of sodium sulfite or thiosul

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