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CAS

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209607-09-0

(E)-3-chloroprop-1-enyldicyclohexylborane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 209607-09-0 Structure

  • Basic information

    1. Product Name: (E)-3-chloroprop-1-enyldicyclohexylborane
    2. Synonyms:
    3. CAS NO:209607-09-0
    4. Molecular Formula:
    5. Molecular Weight: 252.635
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 209607-09-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (E)-3-chloroprop-1-enyldicyclohexylborane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-3-chloroprop-1-enyldicyclohexylborane(209607-09-0)
    11. EPA Substance Registry System: (E)-3-chloroprop-1-enyldicyclohexylborane(209607-09-0)

  • 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: 209607-09-0(Hazardous Substances Data)

209607-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209607-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,6,0 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 209607-09:
(8*2)+(7*0)+(6*9)+(5*6)+(4*0)+(3*7)+(2*0)+(1*9)=130
130 % 10 = 0
So 209607-09-0 is a valid CAS Registry Number.

209607-09-0Upstream product

209607-09-0Relevant articles and documents

The hydroboration of propargyl chloride: A flexible one-pot three-component process easily directed towards the synthesis of (E)-homoallylic alcohols or anti-homoallylic alcohols

Lombardo, Marco,Morganti, Stefano,Trombini, Claudio

, p. 601 - 604 (2001)

The hydroboration of propargyl chloride by means of a dialkylborane affords 3-chloro-propenyl boranes 6 which, in the presence of a quaternary ammonium chloride, rearrange into allylic boranes 9 and 10, precursors of (E)-homoallylic alcohols 7 or anti-homoallylic alcohols 5, respectively. Synthetic protocols for the selective generation of 5 and 7 were developed.

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