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CAS

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119021-79-3

(2-(bromomethyl)phenyl)chloro(2-methylpropyl)borane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 119021-79-3 Structure

  • Basic information

    1. Product Name: (2-(bromomethyl)phenyl)chloro(2-methylpropyl)borane
    2. Synonyms:
    3. CAS NO:119021-79-3
    4. Molecular Formula:
    5. Molecular Weight: 273.408
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 119021-79-3.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: (2-(bromomethyl)phenyl)chloro(2-methylpropyl)borane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-(bromomethyl)phenyl)chloro(2-methylpropyl)borane(119021-79-3)
    11. EPA Substance Registry System: (2-(bromomethyl)phenyl)chloro(2-methylpropyl)borane(119021-79-3)

  • 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: 119021-79-3(Hazardous Substances Data)

119021-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119021-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,2 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 119021-79:
(8*1)+(7*1)+(6*9)+(5*0)+(4*2)+(3*1)+(2*7)+(1*9)=103
103 % 10 = 3
So 119021-79-3 is a valid CAS Registry Number.

119021-79-3Downstream Products

119021-79-3Relevant articles and documents

Erste Synthese eines Benzodihydroborets

Schacht, Wolfgang,Kaufmann, Dieter

, p. 33 - 40 (1988)

The alkali metal mediated 1,4-cyclization of boranes, which yields B-alkyl- and dialkylamino substituted dihydrobenzoboretes, has been investigated.The unknown starting materials for the cyclizations are made by selective monoalkylation or -amination of the dichloroborane (5) with tetramethyl stannane (giving 6a), t-butyllithium (giving the isobutylborane 6b), and diisopropylamine (giving 6c).Only 6c cyclizes, either to the dihydrobenzoborete 7 (with lithium) or its dimer tetrahydrodibenzodiborocine 9 (with potassium).The bora-o-quinodimethane derivative 8, being a valence isomer of 7, could not be trapped.Reaction of 7 with the electrophile boron trichloride yields the ring-opening product 10, with hydrogen chloride a cyclic dichloroborate 12.

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