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CAS

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83721-15-7

bis(3,3-dimethyl-trans-1-buten-1-yl)-N-methyl-N-(2,4,6-trideuteriophenyl)boranamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83721-15-7 Structure

  • Basic information

    1. Product Name: bis(3,3-dimethyl-trans-1-buten-1-yl)-N-methyl-N-(2,4,6-trideuteriophenyl)boranamine
    2. Synonyms:
    3. CAS NO:83721-15-7
    4. Molecular Formula:
    5. Molecular Weight: 286.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83721-15-7.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: bis(3,3-dimethyl-trans-1-buten-1-yl)-N-methyl-N-(2,4,6-trideuteriophenyl)boranamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: bis(3,3-dimethyl-trans-1-buten-1-yl)-N-methyl-N-(2,4,6-trideuteriophenyl)boranamine(83721-15-7)
    11. EPA Substance Registry System: bis(3,3-dimethyl-trans-1-buten-1-yl)-N-methyl-N-(2,4,6-trideuteriophenyl)boranamine(83721-15-7)

  • 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: 83721-15-7(Hazardous Substances Data)

83721-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83721-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,2 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83721-15:
(7*8)+(6*3)+(5*7)+(4*2)+(3*1)+(2*1)+(1*5)=127
127 % 10 = 7
So 83721-15-7 is a valid CAS Registry Number.

83721-15-7Downstream Products

83721-15-7Relevant articles and documents

Mechanism of Cyclization of Divinyl-N-phenylboranamines

Sobieralski, Ted J.,Hancock, Kenneth G.

, p. 7542 - 7548 (2007/10/02)

High-resolution NMR and mass spectral data were used to deduce the mechanism of nonoxidative photocyclization of divinyl-N-phenylboranamines.Cyclization was found to proceed through an excited singlet state conrotatory electrocyclic ring closure between phenyl and ajacent vinyl groups, followed by an intramolecular suprafacial 1,5-hydrogen shift.Such a mechanism was found to be operating in both the divinylboranamines and the dicycloalkenylboranamines.Irradiation in acetonitrile inhibited vinylic photochemical trans-cis isomerization, yielding predominantly the cycloadduct fron starting material vinyl stereochemistry.

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