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2-isopropylamino-3'-methylbenzophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83482-90-0 Structure
  • Basic information

    1. Product Name: 2-isopropylamino-3'-methylbenzophenone
    2. Synonyms:
    3. CAS NO:83482-90-0
    4. Molecular Formula:
    5. Molecular Weight: 253.344
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83482-90-0.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: 2-isopropylamino-3'-methylbenzophenone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-isopropylamino-3'-methylbenzophenone(83482-90-0)
    11. EPA Substance Registry System: 2-isopropylamino-3'-methylbenzophenone(83482-90-0)
  • 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: 83482-90-0(Hazardous Substances Data)

83482-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83482-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,8 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83482-90:
(7*8)+(6*3)+(5*4)+(4*8)+(3*2)+(2*9)+(1*0)=150
150 % 10 = 0
So 83482-90-0 is a valid CAS Registry Number.

83482-90-0Upstream product

83482-90-0Downstream Products

83482-90-0Relevant articles and documents

CLEAVAGE OF THE N-N BOND IN 1-SUBSTITUTED INDAZOLES UNDER THE INFLUENCE OF ARYLLITHIUM COMPOUNDS

Tertov, B. A.,Onishchenko, P. P.,Koshchienko, Yu. V.,Suvorova, G. M.,Malysheva, E. N.

, p. 823 - 826 (1982)

Upon reaction with aryllithium compounds (phenyllithium and m-tolyllithium) m-methyl- and 1-isopropylindazoles undergo cleavage at the N-N bond to give N-substituted 2-aminobenzophenones.The heterocyclic ring of 1-isopropyl-3-phenylindazole also undergoes cleavage at this bond under the influence of phenyllithium.

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