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52340-78-0

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52340-78-0 Usage

Uses

(R,R)-(+)-Hydrobenzoin may be used in the oxyselenenylation step in the multi-step synthesis of cyclopentitols and aminocyclopentitols from cyclopentene. It may also be used as a ligand for the asymmetric addition of diethylzinc to aldehydes in the presence or absence of titanium tetra-isopropoxide to form (R)- or (S)-form of the corresponding secondary alcohol, respectively.

General Description

(R,R)-(+)-Hydrobenzoin is a chiral 1,2-diol useful as a chiral reagent, building block, ligand or auxiliary in asymmetric synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 52340-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,4 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52340-78:
(7*5)+(6*2)+(5*3)+(4*4)+(3*0)+(2*7)+(1*8)=100
100 % 10 = 0
So 52340-78-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H14O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13-16H/t13-,14-/m1/s1

52340-78-0 Well-known Company Product Price

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  • Aldrich

  • (256277)  (R,R)-(+)-Hydrobenzoin  99%, optical purity ee: 99% (HPLC)

  • 52340-78-0

  • 256277-5G

  • 685.62CNY

  • Detail
  • Aldrich

  • (256277)  (R,R)-(+)-Hydrobenzoin  99%, optical purity ee: 99% (HPLC)

  • 52340-78-0

  • 256277-25G

  • 2,520.18CNY

  • Detail

52340-78-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (R,R)-(+)-1,2-Diphenyl-1,2-ethanediol

1.2 Other means of identification

Product number -
Other names (1R,2R)-1,2-diphenylethane-1,2-diol

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:52340-78-0 SDS

52340-78-0Relevant articles and documents

In vitro metabolism of oprozomib, an oral proteasome inhibitor: Role of epoxide hydrolases and cytochrome P450ss

Wang, Zhican,Fang, Ying,Teague, Juli,Wong, Hansen,Morisseau, Christophe,Hammock, Bruce D.,Rock, Dan A.,Wang, Zhengping

, p. 712 - 720 (2017)

Oprozomib is an oral proteasome inhibitor currently under investigation in patients with hematologic malignancies or solid tumors. Oprozomib elicits potent pharmacological actions by forming a covalent bond with the active site N-terminal threonine of the

Asymmetric hydrogenation of 1,4-diketones: facile synthesis of enantiopure 1,4-diarylbutane-1,4-diols

Huang, Fanping,Shao, Pan-Lin,Song, Jingyuan,Wang, Jiang,Zhang, Xumu

supporting information, p. 262 - 265 (2022/01/06)

Owing to the biological significance and great synthetic value of 1,4-diarylbutane-1,4-diols and their derivatives, increasingly considerable attention has been paid to developing effective synthetic methods for chiral 1,4-diarylbutane-1,4-diols. We herei

Ni2P Nanoalloy as an Air-Stable and Versatile Hydrogenation Catalyst in Water: P-Alloying Strategy for Designing Smart Catalysts

Fujita, Shu,Yamaguchi, Sho,Yamasaki, Jun,Nakajima, Kiyotaka,Yamazoe, Seiji,Mizugaki, Tomoo,Mitsudome, Takato

supporting information, p. 4439 - 4446 (2021/02/09)

Non-noble metal-based hydrogenation catalysts have limited practical applications because they exhibit low activity, require harsh reaction conditions, and are unstable in air. To overcome these limitations, herein we propose the alloying of non-noble metal nanoparticles with phosphorus as a promising strategy for developing smart catalysts that exhibit both excellent activity and air stability. We synthesized a novel nickel phosphide nanoalloy (nano-Ni2P) with coordinatively unsaturated Ni active sites. Unlike conventional air-unstable non-noble metal catalysts, nano-Ni2P retained its metallic nature in air, and exhibited a high activity for the hydrogenation of various substrates with polar functional groups, such as aldehydes, ketones, nitriles, and nitroarenes to the desired products in excellent yields in water. Furthermore, the used nano-Ni2P catalyst was easy to handle in air and could be reused without pretreatment, providing a simple and clean catalyst system for general hydrogenation reactions.

A convenient pinacol coupling of diaryl ketones with B2pin2viapyridine catalysis

Jo, Junhyuk,Kim, Seonyul,Choi, Jun-Ho,Chung, Won-Jin

supporting information, p. 1360 - 1363 (2021/02/22)

A convenient, pyridine-boryl radical-mediated pinacol coupling of diaryl ketones is developed. In contrast to the conventional pinacol coupling that requires sensitive reducing metal, the current method employs a stable diboron reagent and pyridine Lewis base catalyst for the generation of a ketyl radical. The newly developed process is operationally simple, and the desired diols are produced with excellent efficiency in up to 99% yield within 1 hour. The superior reactivity of diaryl ketone was observed over monoaryl carbonyl compounds and analyzed by DFT calculations, which suggests the necessity of both aromatic rings for the maximum stabilization of the transition states.

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