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3-Isoxazolidinecarboxylicacid,5-ethoxy-2-methyl-,ethylester,cis-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83095-76-5

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83095-76-5 Usage

Chemical compound

3-Isoxazolidinecarboxylic acid, 5-ethoxy-2-methyl-, ethyl ester, cis-(9CI)

Derivative of

Isoxazolidinecarboxylic acid

Configuration

cis

Functional groups

ethoxy group and methyl group

Potential applications

pharmaceutical and chemical industries

Unique structure and properties

may have specific uses and potential benefits

Further research

needed for analysis of specific uses and benefits in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 83095-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,9 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83095-76:
(7*8)+(6*3)+(5*0)+(4*9)+(3*5)+(2*7)+(1*6)=145
145 % 10 = 5
So 83095-76-5 is a valid CAS Registry Number.

83095-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,5R)-5-Ethoxy-2-methyl-isoxazolidine-3-carboxylic acid ethyl ester

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:83095-76-5 SDS

83095-76-5Downstream Products

83095-76-5Relevant academic research and scientific papers

Determination of Configuration and Conformation of Isoxazolidines by Nuclear Overhauser Effect Difference Spectroscopy

DeShong, Philip,Dicken, C. Michael,Staib, Ronald R.,Freyer, Alan J.,Weinreb, Steven M.

, p. 4397 - 4403 (2007/10/02)

The configurations of isoxazolidines 2, 3, 5, 7, and 10-12 have been assigned by analysis of NMR coupling constants and by nuclear Overhauser effect difference spectroscopy (NOEDS).The preferred solution conformations of isoxazolidines 3 and 5 were determined to be as in 3A/5A.It is proposed that these conformations are adopted to take advantage of the anomeric effect and to alleviate the unfavorable stereoelectronic lone pair-lone pair interaction in the N-O portion of the molecule (gauche effect).

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