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m-Diallylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52448-03-0 Structure
  • Basic information

    1. Product Name: m-Diallylbenzene
    2. Synonyms: m-Diallylbenzene
    3. CAS NO:52448-03-0
    4. Molecular Formula: C12H14
    5. Molecular Weight: 158.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52448-03-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 220-221°C
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: m-Diallylbenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: m-Diallylbenzene(52448-03-0)
    11. EPA Substance Registry System: m-Diallylbenzene(52448-03-0)
  • 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: 52448-03-0(Hazardous Substances Data)

52448-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52448-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,4 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52448-03:
(7*5)+(6*2)+(5*4)+(4*4)+(3*8)+(2*0)+(1*3)=110
110 % 10 = 0
So 52448-03-0 is a valid CAS Registry Number.

52448-03-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis(prop-2-enyl)benzene

1.2 Other means of identification

Product number -
Other names m-Diallylbenzene

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:52448-03-0 SDS

52448-03-0Downstream Products

52448-03-0Relevant articles and documents

Nickel-catalyzed heck-type reactions of benzyl chlorides and simple olefins

Matsubara, Ryosuke,Gutierrez, Alicia C.,Jamison, Timothy F.

supporting information; experimental part, p. 19020 - 19023 (2011/12/21)

Nickel-catalyzed intermolecular benzylation and heterobenzylation of unactivated alkenes to provide functionalized allylbenzene derivatives are described. A wide range of both the benzyl chloride and alkene coupling partners are tolerated. In contrast to analogous palladium-catalyzed variants of this process, all reactions described herein employ electronically unbiased aliphatic olefins (including ethylene), proceed at room temperature, and provide 1,1-disubstituted olefins over the more commonly observed 1,2-disubstituted olefins with very high selectivity.

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