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136828-09-6

5-Oxazolidinone, 4-(2-oxo-2-phenylethyl)-2,2-bis(trifluoromethyl)-, (S)- is a complex organic compound with the molecular formula C12H8F6N2O3. It is a chiral molecule, with the (S)-configuration indicating the specific arrangement of atoms in the molecule. 5-Oxazolidinone, 4-(2-oxo-2-phenylethyl)-2,2-bis(trifluoromethyl)-, (S)- is characterized by a 5-oxazolidinone ring, which is a five-membered heterocyclic ring containing an oxygen and a nitrogen atom. The molecule also features a 2-oxo-2-phenylethyl group, which is a phenyl-ethyl moiety with a carbonyl group, and two trifluoromethyl groups, which are methyl groups with three fluorine atoms. 5-Oxazolidinone, 4-(2-oxo-2-phenylethyl)-2,2-bis(trifluoromethyl)-, (S)- is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a building block for more complex molecules.

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  • 136828-09-6 Structure

  • Basic information

    1. Product Name: 5-Oxazolidinone, 4-(2-oxo-2-phenylethyl)-2,2-bis(trifluoromethyl)-, (S)-
    2. Synonyms:
    3. CAS NO:136828-09-6
    4. Molecular Formula: C13H9F6NO3
    5. Molecular Weight: 341.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 136828-09-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-Oxazolidinone, 4-(2-oxo-2-phenylethyl)-2,2-bis(trifluoromethyl)-, (S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Oxazolidinone, 4-(2-oxo-2-phenylethyl)-2,2-bis(trifluoromethyl)-, (S)-(136828-09-6)
    11. EPA Substance Registry System: 5-Oxazolidinone, 4-(2-oxo-2-phenylethyl)-2,2-bis(trifluoromethyl)-, (S)-(136828-09-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 136828-09-6(Hazardous Substances Data)

136828-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136828-09-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,2 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 136828-09:
(8*1)+(7*3)+(6*6)+(5*8)+(4*2)+(3*8)+(2*0)+(1*9)=146
146 % 10 = 6
So 136828-09-6 is a valid CAS Registry Number.

136828-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(benzoylmethyl)-2,2-bis(trifluoromethyl)-1,3-oxazolidin-5-one

1.2 Other means of identification

Product number -
Other names (S)-4-(2-Oxo-2-phenyl-ethyl)-2,2-bis-trifluoromethyl-oxazolidin-5-one

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:136828-09-6 SDS

136828-09-6Relevant articles and documents

Synthesis of γ-oxo α-amino acids from L-aspartic acid

Golubev, Alexander S.,Sewald, Norbert,Burger, Klaus

, p. 14757 - 14776 (2007/10/03)

The synthesis of different γ-oxo α-amino acids from hexafluoroacetone protected L-aspartic acid chloride 1 via Stille cross coupling reaction is described. Stille reaction of 1 with vinyltributyltin followed by Lewis acid catalyzed intramolecular Michael addition provides access to 4-substituted pipecolic acid derivatives. An efficient synthesis of 5-hydroxy-4-oxo-L-norvaline 7 and a new approach to the 4-oxo-L-ornithine skeleton starting from 1 have been elaborated.

Hexafluoroacetone as Protecting Group and Activation Reagent in Amino Acid and Peptide Chemistry, 7. - Synthesis of γ-Oxo α-Amino Acid Derivatives from Aspartic Acid

Burger, Klaus,Rudolph, Martin,Neuhauser, Horst

, p. 1365 - 1368 (2007/10/02)

Optically pure γ-oxo α-amino acids are obtained on reaction of acid chloride 2 with aromatic and heteroaromatic compounds under Friedel-Crafts conditions.Key Words: Aspartic acid / Hexafluoroacetone / Friedel-Crafts acylation / γ-Oxo α-amino acids / Amino

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