Welcome to LookChem.com Sign In|Join Free

CAS

  • or

352535-72-9

Post Buying Request

352535-72-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

352535-72-9 Usage

Description

(R)-(+)-5,5-DIPHENYL-4-ISOBUTYL-2-OXAZOLIDINONE is a chiral chemical compound belonging to the class of oxazolidinones. It is characterized by its specific spatial arrangement of atoms, which gives it a non-superimposable mirror image. With a molecular formula of C19H23NO2 and a molecular weight of 297.39 g/mol, this compound is widely recognized for its applications in asymmetric synthesis and potential biological and pharmacological properties.

Uses

Used in Pharmaceutical Industry:
(R)-(+)-5,5-DIPHENYL-4-ISOBUTYL-2-OXAZOLIDINONE is used as a chiral auxiliary for the production of enantiomerically pure compounds. Its ability to create pure enantiomers is crucial in the development of pharmaceuticals, as the different forms of a molecule can have distinct effects on biological systems.
Used in Chemical Synthesis:
In the field of chemical synthesis, (R)-(+)-5,5-DIPHENYL-4-ISOBUTYL-2-OXAZOLIDINONE serves as a valuable chiral auxiliary. It aids in the creation of complex molecules with precise stereochemistry, which is essential for the effectiveness, safety, and selectivity of various chemical products.
Used in Enzyme Inhibition Research:
(R)-(+)-5,5-DIPHENYL-4-ISOBUTYL-2-OXAZOLIDINONE has been studied for its potential to inhibit certain enzymes. This property makes it a candidate for further research and development in the creation of new pharmaceuticals targeting specific enzyme pathways.
Used in Drug Development:
(R)-(+)-5,5-DIPHENYL-4-ISOBUTYL-2-OXAZOLIDINONE's potential biological and pharmacological properties make it a promising candidate for the development of new drugs. Its ability to inhibit enzymes and its chiral nature could lead to the creation of innovative therapeutic agents for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 352535-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,3 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 352535-72:
(8*3)+(7*5)+(6*2)+(5*5)+(4*3)+(3*5)+(2*7)+(1*2)=139
139 % 10 = 9
So 352535-72-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H21NO2/c1-14(2)13-17-19(22-18(21)20-17,15-9-5-3-6-10-15)16-11-7-4-8-12-16/h3-12,14,17H,13H2,1-2H3,(H,20,21)/t17-/m1/s1

352535-72-9SDS

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 (4R)-4-(2-methylpropyl)-5,5-diphenyl-1,3-oxazolidin-2-one

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:352535-72-9 SDS

352535-72-9Downstream Products

352535-72-9Relevant articles and documents

A short synthesis of (S)-α-(diphenylmethyl)alkyl amines from amino acids

O'Hagan, David,Tavasli, Mustafa

, p. 1189 - 1192 (2007/10/03)

A range of (S)-α-(diphenylmethyl)alkyl amines were prepared from the corresponding (S)-α-amino acid ester hydrochlorides. These amines were derived by direct hydrogenation of their precursor oxazolidinones.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 352535-72-9