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[(tris(4,4-dimethyl-2-oxazolinyl)phenylborate)RhH2(CO)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1402852-02-1 Structure
  • Basic information

    1. Product Name: [(tris(4,4-dimethyl-2-oxazolinyl)phenylborate)RhH2(CO)]
    2. Synonyms:
    3. CAS NO:1402852-02-1
    4. Molecular Formula:
    5. Molecular Weight: 515.222
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1402852-02-1.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: [(tris(4,4-dimethyl-2-oxazolinyl)phenylborate)RhH2(CO)](CAS DataBase Reference)
    10. NIST Chemistry Reference: [(tris(4,4-dimethyl-2-oxazolinyl)phenylborate)RhH2(CO)](1402852-02-1)
    11. EPA Substance Registry System: [(tris(4,4-dimethyl-2-oxazolinyl)phenylborate)RhH2(CO)](1402852-02-1)
  • 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: 1402852-02-1(Hazardous Substances Data)

1402852-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1402852-02-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,8,5 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1402852-02:
(9*1)+(8*4)+(7*0)+(6*2)+(5*8)+(4*5)+(3*2)+(2*0)+(1*2)=121
121 % 10 = 1
So 1402852-02-1 is a valid CAS Registry Number.

1402852-02-1Downstream Products

1402852-02-1Relevant articles and documents

Acceptorless photocatalytic dehydrogenation for alcohol decarbonylation and imine synthesis

Ho, Hung-An,Manna, Kuntal,Sadow, Aaron D.

, p. 8607 - 8610 (2012)

It has come to light: Renewed interest in conversions of highly oxygenated materials has motivated studies of the organometallic-catalyzed photocatalytic dehydrogenative decarbonylation of primary alcohols into alkanes, CO, and H2 (see scheme). Methanol, ethanol, benzyl alcohol, and cyclohexanemethanol are readily decarbonylated. The photocatalysts are also active for amine dehydrogenation to give N-alkyl aldimines and H2.

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