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113614-48-5

(3S,5S)-3-(4-chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methyl-5-phenyl-1,2-oxazolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 113614-48-5 Structure

  • Basic information

    1. Product Name: (3S,5S)-3-(4-chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methyl-5-phenyl-1,2-oxazolidine
    2. Synonyms: (3S,5S)-3-(4-Chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methyl-5-phenyl-1,2-oxazolidine; isoxazolidine, 3-(4-chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methyl-5-phenyl-, (3S,5S)-
    3. CAS NO:113614-48-5
    4. Molecular Formula: C20H20ClN3O
    5. Molecular Weight: 353.8453
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113614-48-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 524.5°C at 760 mmHg
    3. Flash Point: 271°C
    4. Appearance: N/A
    5. Density: 1.23g/cm3
    6. Vapor Pressure: 4.3E-11mmHg at 25°C
    7. Refractive Index: 1.627
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3S,5S)-3-(4-chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methyl-5-phenyl-1,2-oxazolidine(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3S,5S)-3-(4-chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methyl-5-phenyl-1,2-oxazolidine(113614-48-5)
    12. EPA Substance Registry System: (3S,5S)-3-(4-chlorophenyl)-3-(1H-imidazol-1-ylmethyl)-2-methyl-5-phenyl-1,2-oxazolidine(113614-48-5)

  • 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: 113614-48-5(Hazardous Substances Data)

113614-48-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113614-48-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,6,1 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 113614-48:
(8*1)+(7*1)+(6*3)+(5*6)+(4*1)+(3*4)+(2*4)+(1*8)=95
95 % 10 = 5
So 113614-48-5 is a valid CAS Registry Number.

113614-48-5SDS

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 (3S,5S)-3-(4-chlorophenyl)-3-(imidazol-1-ylmethyl)-2-methyl-5-phenyl-1,2-oxazolidine

1.2 Other means of identification

Product number -
Other names BBNVZZVNBCNJEY-VQTJNVASSA

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:113614-48-5 SDS

113614-48-5Downstream Products

113614-48-5Relevant articles and documents

1,3-Dipolar Cycloaddition Reactions of 1-Aryl-N-methyl-2-(1H-azol-1-yl)-ethanimine N-Oxides to Olefins

Mullen, George B.,Bennett, Grace A.,Swift, Patricia A.,Marinyak, David M.,Dormer, Peter G.,Georgiev, Vassil St.

, p. 105 - 107 (2007/10/02)

The regio- and stereoselectivity of the 1,3-dipolar cycloaddition reaction of 1-aryl-N-methyl-2-(1H-azol-1-yl)ethanimine N-oxides 6 to monosubstituted olefins 7 were investigated.The reaction is regioselective, leading to the corresponding C-5 substituted isoxazolidines 8/9 as cis/trans diastereomeric mixtures.The cis isomers, which are the predominant species of the mixtures, are readily separated by flash chromatography on neutral silica gel.

Studies on antifungal agents. 23. Novel substituted 3,5-diphenyl3-(1H-imidazol-1-ylmethyl)-2-alkylisoxazolidine derivatives

Mullen,DeCory,Mitchell,Allen,Kinsolving,Georgiev

, p. 2008 - 2014 (2007/10/02)

The synthesia and antifungal activity of a novel series of substituted 3,5-diphenyl-3-(1H-imidazol-1-ylmethyl)-2-alkylisoxazolidine derivatives are described. The synthesis of the title compounds was accomplished via a 1,3 dipolar cycloaddition reaction o

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