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Oxiranecarboxylic acid, 3-(4-nitrophenyl)-, ethyl ester, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54679-39-9

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54679-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54679-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,7 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54679-39:
(7*5)+(6*4)+(5*6)+(4*7)+(3*9)+(2*3)+(1*9)=159
159 % 10 = 9
So 54679-39-9 is a valid CAS Registry Number.

54679-39-9SDS

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 ethyl (2R,3S)-3-(4-nitrophenyl)oxirane-2-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:54679-39-9 SDS

54679-39-9Downstream Products

54679-39-9Relevant academic research and scientific papers

Facile construction of three-membered rings via benzyne-promoted Darzens-type reaction of tertiary amines

Xu, Ya-Nan,Tian, Shi-Kai

, p. 1632 - 1638 (2019)

A range of tertiary amines having electron-withdrawing groups were activated in situ by benzyne, generated from 2-(trimethylsilyl)phenyl triflate and a fluoride source, and participated in the Darzens-type reaction with carbonyl compounds, imines, and vinyl ketones to afford structurally diverse epoxides, aziridines, and cyclopropanes, respectively, in moderate to excellent yields with high trans-selectivity. The reaction involves in situ formation of unstrained ammonium ylides from tertiary amines and benzyne, proceeds in the absence of transition metals and strong bases, and tolerates a wide variety of functional groups.

β-alanine derivates

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Page/Page column 22, (2010/02/14)

Alkanoic acid derivatives of formula (1) are described: [in-line-formulae]Ar1(Alka)rL1Ar2CH(R1)C(Ra)(Ra′)R??(1)[/in-line-formulae]Ar1 is an optionally subst

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