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1448901-19-6

(1,3-bis(2,6-diisopropylphenyl)-1H-imidazol-3-ium-2-yl)(2-ethoxy-2-oxoethyl)dihydroborate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1448901-19-6 Structure

  • Basic information

    1. Product Name: (1,3-bis(2,6-diisopropylphenyl)-1H-imidazol-3-ium-2-yl)(2-ethoxy-2-oxoethyl)dihydroborate
    2. Synonyms:
    3. CAS NO:1448901-19-6
    4. Molecular Formula:
    5. Molecular Weight: 488.521
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1448901-19-6.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: (1,3-bis(2,6-diisopropylphenyl)-1H-imidazol-3-ium-2-yl)(2-ethoxy-2-oxoethyl)dihydroborate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1,3-bis(2,6-diisopropylphenyl)-1H-imidazol-3-ium-2-yl)(2-ethoxy-2-oxoethyl)dihydroborate(1448901-19-6)
    11. EPA Substance Registry System: (1,3-bis(2,6-diisopropylphenyl)-1H-imidazol-3-ium-2-yl)(2-ethoxy-2-oxoethyl)dihydroborate(1448901-19-6)

  • 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: 1448901-19-6(Hazardous Substances Data)

1448901-19-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1448901-19-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,9,0 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1448901-19:
(9*1)+(8*4)+(7*4)+(6*8)+(5*9)+(4*0)+(3*1)+(2*1)+(1*9)=176
176 % 10 = 6
So 1448901-19-6 is a valid CAS Registry Number.

1448901-19-6Downstream Products

1448901-19-6Relevant articles and documents

Insertion of reactive rhodium carbenes into boron-hydrogen bonds of stable N-heterocyclic carbene boranes

Li, Xiben,Curran, Dennis P.

, p. 12076 - 12081 (2013)

Readily available rhodium(II) salts catalyze reactions between NHC-boranes (NHC-BH3) and diazocarbonyl compounds (N2CRCOR′). Stable α-NHC-boryl carbonyl compounds (NHC-BH2-CHRCOR′) are isolated in good yields. The reaction is a reliable way to make boron-carbon bonds with good tolerance for variation in both the NHC-borane and diazocarbonyl components. It presumably occurs by insertion of a transient rhodium carbene into a boron-hydrogen bond of the NHC-borane. Competitive experiments show that a typical NHC-borane is highly reactive toward rhodium carbenes.

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