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CAS

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79213-82-4

4-(2,2-dimethyl-4-phenyl-2,5-dihydro-1,3-oxazol-5-yl)-N,N-dimethylaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 79213-82-4 Structure

  • Basic information

    1. Product Name: 4-(2,2-dimethyl-4-phenyl-2,5-dihydro-1,3-oxazol-5-yl)-N,N-dimethylaniline
    2. Synonyms: 3-Oxazoline, 2,2-dimethyl-5-(p-(dimethylamino)phenyl)-4-phenyl-; Benzenamine, N,N-dimethyl-4-(2,5-dihydro-2,2-dimethyl-4-phenyl-5-oxazolyl)-; N,N-Dimethyl-4-(2,5-dihydro-2,2-dimethyl-4-phenyl-5-oxazolyl)benzenamine
    3. CAS NO:79213-82-4
    4. Molecular Formula: C19H22N2O
    5. Molecular Weight: 294.3908
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79213-82-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 425.2°C at 760 mmHg
    3. Flash Point: 211°C
    4. Appearance: N/A
    5. Density: 1.06g/cm3
    6. Vapor Pressure: 1.95E-07mmHg at 25°C
    7. Refractive Index: 1.568
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-(2,2-dimethyl-4-phenyl-2,5-dihydro-1,3-oxazol-5-yl)-N,N-dimethylaniline(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-(2,2-dimethyl-4-phenyl-2,5-dihydro-1,3-oxazol-5-yl)-N,N-dimethylaniline(79213-82-4)
    12. EPA Substance Registry System: 4-(2,2-dimethyl-4-phenyl-2,5-dihydro-1,3-oxazol-5-yl)-N,N-dimethylaniline(79213-82-4)

  • 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: 79213-82-4(Hazardous Substances Data)

79213-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79213-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,1 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79213-82:
(7*7)+(6*9)+(5*2)+(4*1)+(3*3)+(2*8)+(1*2)=144
144 % 10 = 4
So 79213-82-4 is a valid CAS Registry Number.

79213-82-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2,2-dimethyl-4-phenyl-5H-1,3-oxazol-5-yl)-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names 4-(2,5-Dihydro-2,2-dimethyl-4-phenyl-5-oxazolyl)-N,N-dimethylbenzenamine

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:79213-82-4 SDS

79213-82-4Relevant articles and documents

66. Synthese und Reaktionen des 5--2,2-dimethyl-4-phenyl-3-oxazolins

Foricher, Joseph,Montavon, Francois,Pfoertner, Karl-Heinz,Schoenholzer, Peter

, p. 592 - 599 (2007/10/02)

Synthesis and Reactions of 5--2,2-dimethyl-4-phenyl-3-oxazoline.The title compound 8 has been synthesized in a one-pot reaction of 4'-(dimethylamino)benzoin (4) with 2-propanone and NH3.The preparation of the intermediate 4 from 3 is the first example of an acid-catalyzed transformation of the stable benzoin 3 into the corresponding less stable benzoin 4.Structures and yields of various by-products occuring under different reaction conditions during the synthesis of 8 from 4 are given.The O-atom of the 3-oxazoline ring in 8 could be replaced by S from P2S5 yielding the 3-thiazoline 14.Separation of the enantiomers of the racemate 8 could only be performed by transforming them into the trimethylanilinium salts 8b and 8c of (-)- and (+)-10-camphorsulfonic acid, respectively.Solid NaOAc in boiling toluene caused the precipitation of the 10-camphorsulfonic acids from the quaternary ammonium salts as sodium salts and the removing of the third methyl group from the quaternary ammonium salts as AcOMe to give the enantiomers (-)-(5S)-8 and (+)-(5R)-8.Their absolute configurations are deduced from an X-ray analysis of 8b.

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