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13383-32-9

7-chloro-7-phenylbicyclo[4.1.0]heptane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13383-32-9 Structure

  • Basic information

    1. Product Name: 7-chloro-7-phenylbicyclo[4.1.0]heptane
    2. Synonyms:
    3. CAS NO:13383-32-9
    4. Molecular Formula: C13H15Cl
    5. Molecular Weight: 206.7112
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13383-32-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 294.8°C at 760 mmHg
    3. Flash Point: 120.1°C
    4. Appearance: N/A
    5. Density: 1.14g/cm3
    6. Vapor Pressure: 0.00279mmHg at 25°C
    7. Refractive Index: 1.576
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 7-chloro-7-phenylbicyclo[4.1.0]heptane(CAS DataBase Reference)
    11. NIST Chemistry Reference: 7-chloro-7-phenylbicyclo[4.1.0]heptane(13383-32-9)
    12. EPA Substance Registry System: 7-chloro-7-phenylbicyclo[4.1.0]heptane(13383-32-9)

  • 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: 13383-32-9(Hazardous Substances Data)

13383-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13383-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,8 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13383-32:
(7*1)+(6*3)+(5*3)+(4*8)+(3*3)+(2*3)+(1*2)=89
89 % 10 = 9
So 13383-32-9 is a valid CAS Registry Number.

13383-32-9SDS

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 7-chloro-7-phenylbicyclo[4.1.0]heptane

1.2 Other means of identification

Product number -
Other names Bicyclo[4.1.0]heptane,7-chloro-7-phenyl

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:13383-32-9 SDS

13383-32-9Downstream Products

13383-32-9Relevant articles and documents

Enthalpy versus entropy in chlorocarbene/alkene addition reactions

Moss, Robert A.,Wang, Lei,Zhang, Min,Skalit, Christopher,Krogh-Jespersen, Karsten

, p. 5634 - 5635 (2008)

We report the first measured activation parameters for the additions of CCl2 and CClF to simple alkenes and demonstrate the existence of enthalpic barriers for CCl2 additions to cyclohexene and 1-hexene. With these two alkenes, addit

Complexes and Negative Activation Energies in Arylhalocarbene/Alkene Additions: Activation Parameter Dependence on Alkane Solvent Chain Length

Wang, Lei,Moss, Robert A.,Krogh-Jespersen, Karsten

supporting information, p. 4216 - 4225 (2017/04/28)

Activation parameters for the additions of PhCCl, F5-PhCCl, and 3,5-dinitro-PhCCl to tetramethylethylene, cyclohexene, and 1-hexene have been determined in decane. With the exception of two carbene/alkene combinations, Arrhenius correlations of

The reaction of benzotrihalides and benzal halides with magnesium. Synthetic and mechanistic studies

Ashby, E. C.,Al-Fekri, Dheya M.

, p. 275 - 292 (2007/10/02)

The benzotrihalides (PhCX3) where X = Cl, Br, and F were allowed to react with magnesium in THF at room temperature.When the halide was chloride or bromide, the trihalide gave diphenylacetylene in high yield in addition to several minor products which were identified.No reaction was observed when the halide was fluoride.When the corresponding dichloride was allowed to react with magnesium in THF, stilbene was formed as the major product.The possible mechanisms for these reactions are discussed.

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