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3-Oxazolidineacetic acid, 2-oxo-4-phenyl-, methyl ester, (S)- is a complex organic compound with the chemical formula C11H11NO4. It is a chiral molecule, with the (S)- configuration indicating the specific arrangement of atoms in the molecule. 3-Oxazolidineacetic acid, 2-oxo-4-phenyl-, methyl ester, (S)- is characterized by an oxazolidine ring, which is a five-membered ring containing an oxygen and a nitrogen atom, and a phenyl group attached to a 2-oxo-4-phenyl-2-oxazolidineacetic acid structure. The methyl ester group is attached to the carboxylic acid functionality, making it a derivative of the parent acid. 3-Oxazolidineacetic acid, 2-oxo-4-phenyl-, methyl ester, (S)- is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a synthetic intermediate.

139731-96-7

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139731-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139731-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,7,3 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 139731-96:
(8*1)+(7*3)+(6*9)+(5*7)+(4*3)+(3*1)+(2*9)+(1*6)=157
157 % 10 = 7
So 139731-96-7 is a valid CAS Registry Number.

139731-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (4(S)-phenyloxazolidin-2-on-3-yl)acetate

1.2 Other means of identification

Product number -
Other names ((S)-2-Oxo-4-phenyl-oxazolidin-3-yl)-acetic acid methyl 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:139731-96-7 SDS

139731-96-7Relevant academic research and scientific papers

COMPOSITIONS AND METHODS FOR TREATING BRAIN INJURY

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Page/Page column 54, (2019/04/11)

Compounds, and compositions, methods, and uses thereof, are described herein for treating brain injuries.

COMPOSITIONS AND METHODS FOR TREATING NEURODEGENERATIVE DISEASES

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Page/Page column 54, (2015/12/23)

Compounds, and compositions, methods, and uses thereof, are described herein for treating neurodegenerative diseases and disorders. In particular, vasopressin receptor modulators, and compositions, methods and uses thereof, are described herein for treati

METHODS FOR TREATING POST TRAUMATIC STRESS DISORDER

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Page/Page column 46, (2012/01/15)

Compounds and compositions are described herein for treating post tramatic stress disorder.

BETA-LACTAM CANNABINOID RECEPTOR MODULATORS

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Page/Page column 84-85, (2008/06/13)

Described herein are substituted 2-(azetidin-2-on-l-yl)alkanoic acids, alkanedioic acids and 2-hydroxyalkyl alkanoic acids, and 2-acyl alkanoic acids, and derivatives thereof, that are capable of modulating activity at the cannabinoid-1 (CBl) and/or canna

β -LACTAMYL VASOPRESSIN V2 ANTAGONISTS

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Page/Page column 63, (2010/11/28)

β-lactamyl alkanoic acids and pharmaceutical compositions thereof are described. Methods for treating various diseases and disease states using one or more β-lactamyl alkanoic acids are also described. Substituted 2-(azetidin-2-on-l-yl)alkanedioic acids,

HYDROXY AND KETO-SUBSTITUTED β-LACTAMYL ALKANEDIOIC ACIDS

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Page/Page column 48, (2010/11/28)

3-Hydroxy and 3-keto substituted 2-(azetidin-2-on-l-yl)alkanedioic acids, and analogs and derivatives thereof are described. Methods for using 3-hydroxy and 3-keto substituted 2-(azetidin-2-on-l-yl)alkanedioic acids, and analogs and derivatives thereof, i

BETA-LACTAMYLALKANOIC ACIDS FOR TREATING PREMENSTRUAL DISORDERS

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Page/Page column 22, (2008/06/13)

0-lactamyl alkanoic acids are described. Methods for treating various premenstrual disorders using or more β-lactamyl alkanoic acids are also described.

3-SUBSTITUTED β-LACTAMYL VASOPRESSIN V1A ANTAGONISTS

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Page/Page column 40-41, (2008/06/13)

Novel 2-(azetidin-2-on-1-yl)alkanedioic acids and derivatives thereof are described. Methods for using 2-(azetidin-2-on-l-yl)alkanedioic acids and derivatives thereof in the treatment of disease states responsive to antagonism of the vasopressin V1a

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