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propan-2-yl 3-phenyloxirane-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65017-34-7

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65017-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65017-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,1 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65017-34:
(7*6)+(6*5)+(5*0)+(4*1)+(3*7)+(2*3)+(1*4)=107
107 % 10 = 7
So 65017-34-7 is a valid CAS Registry Number.

65017-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name propan-2-yl 3-phenyloxirane-2-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Phenyloxiranecarboxylic acid1-methylethyl ester

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:65017-34-7 SDS

65017-34-7Upstream product

65017-34-7Downstream Products

65017-34-7Relevant academic research and scientific papers

A mononuclear manganese complex of a tetradentate nitrogen ligand - Synthesis, characterizations, and application in the asymmetric epoxidation of olefins

Shen, Duyi,Miao, Chengxia,Wang, Shoufeng,Xia, Chungu,Sun, Wei

supporting information, p. 5777 - 5782 (2015/02/19)

A new chiral manganese complex (C1) bearing a tetradentate nitrogen ligand containing chiral bipyrrolidine and benzimidazole moieties was prepared. The structure of C1 was confirmed by ESI-MS and crystallography. This manganese complex is an active catalyst for the asymmetric epoxidation of various olefins with excellent conversion (up to 99%) and high enantiomeric excess (up to 96%ee) with hydrogen peroxide as the oxidant in the presence of 2-ethylhexanoic acid or acetic acid. Compared with previous structurally similar manganese complexes with different diamine backbones (C2, cyclohexanediamine; C3, diamine from L-proline), C1 showed improved asymmetric induction, especially for simple olefins such as styrene derivatives and substituted chromene. The possible reasons for the improvement of the ee values are discussed in the text on the basis of the crystal structures of the manganese complexes.

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