Basic information

Product Name: 2-Oxazolidinone, 3,5-dimethyl-5-phenyl-
Synonyms:
CAS NO:62432-74-0
Molecular Formula: C11H13NO2
Molecular Weight: 191.23
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-Oxazolidinone, 3,5-dimethyl-5-phenyl-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Oxazolidinone, 3,5-dimethyl-5-phenyl-(62432-74-0)
EPA Substance Registry System: 2-Oxazolidinone, 3,5-dimethyl-5-phenyl-(62432-74-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 62432-74-0(Hazardous Substances Data)

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62432-74-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62432-74-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,3 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62432-74:
(7*6)+(6*2)+(5*4)+(4*3)+(3*2)+(2*7)+(1*4)=110
110 % 10 = 0
So 62432-74-0 is a valid CAS Registry Number.

62432-74-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	3,5-dimethyl-5-phenyl-1,3-oxazolidin-2-one

1.2 Other means of identification

Product number	-
Other names	3,5-dimethyl-5-phenyl-oxazolidin-2-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).

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62432-74-0Relevant academic research and scientific papers

α-Nitrogenated organolithium compounds from α-amidomethyl and α-aminomethyl sulfones

Alonso, Diego A.,Alonso, Emma,Najera, Carmen,Ramon, Diego J.,Yus, Miguel

, p. 4835 - 4856 (2007/10/03)

Successive reaction of α-amidomethyl sulfones 7a,b, derived from primary amides, with n-butyllithium and primary alkyl bromides (CH2 = CHCH2Br, CH2 = CMeCH2Br, CH2 = CBrCH2Br, CH ≡ CCH

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