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(3S,4R)-4-Benzyl-3-(3-methylpentanoyl)-oxazolidin-2-one is a chiral chemical compound belonging to the oxazolidinone class. It features a stereocenter at the third and fourth positions, and is characterized by the presence of a benzyl group and a methylpentanoyl group. These structural elements confer specific reactivity and properties, making it a valuable intermediate in various organic synthesis processes. Its oxazolidinone structure also positions it as a potential candidate for medicinal chemistry research and drug development.

228267-64-9

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228267-64-9 Usage

Uses

Used in Pharmaceutical Synthesis:
(3S,4R)-4-Benzyl-3-(3-methylpentanoyl)-oxazolidin-2-one is used as an intermediate in the synthesis of pharmaceuticals due to its unique structural features and reactivity. Its benzyl and methylpentanoyl groups contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Synthesis:
In the agrochemical industry, (3S,4R)-4-benzyl-3-(3-methylpentanoyl)-oxazolidin-2-one serves as an intermediate for the synthesis of agrochemicals, potentially leading to the creation of new pesticides or other agricultural products that can improve crop yields and protect against pests.
Used in Medicinal Chemistry Research:
(3S,4R)-4-Benzyl-3-(3-methylpentanoyl)-oxazolidin-2-one is utilized in medicinal chemistry research for its potential applications in drug development. Its oxazolidinone structure makes it a promising candidate for the design and synthesis of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 228267-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,2,6 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 228267-64:
(8*2)+(7*2)+(6*8)+(5*2)+(4*6)+(3*7)+(2*6)+(1*4)=149
149 % 10 = 9
So 228267-64-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H21NO3/c1-3-12(2)9-15(18)17-14(11-20-16(17)19)10-13-7-5-4-6-8-13/h4-8,12,14H,3,9-11H2,1-2H3/t12-,14+/m0/s1

228267-64-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R)-4-benzyl-3-[(3S)-3-methylpentanoyl]-1,3-oxazolidin-2-one

1.2 Other means of identification

Product number -
Other names 2-Oxazolidinone,3-[(3S)-3-methyl-1-oxopentyl]-4-(phenylmethyl)-,(4R)

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:228267-64-9 SDS

228267-64-9Relevant academic research and scientific papers

Total synthesis of (+)-belactosin A.

Armstrong, Alan,Scutt, James N

, p. 510 - 511 (2007/10/03)

A concise first total synthesis of the antitumour antibiotic belactosin A is reported, involving coupling of beta-lactone carboxylic acid 3 with N-Ala-aminocyclopropyl alanine 11.

Absolute configuration of the four stereoisomers of valnoctamide (2- ethyl-3-methyl valeramide), a potentially new stereospecific antiepileptic and CNS drug

Roeder, Michael,Spiegelstein, Ofer,Schurig, Volker,Bialer, Meir,Yagen, Boris

, p. 841 - 853 (2007/10/03)

Valnoctamide (2-ethyl-3-methyl valeramide, Nirvanil, VCD), a mild tranquilizer endowed with anticonvulsant properties, exhibits diastereoselective and enantioselective pharmacokinetics in healthy subjects and epileptic patients. The purpose of this paper

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