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75898-02-1

(CH3)(C6H5)C3N2(OH)C(O)C6H5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 75898-02-1 Structure

  • Basic information

    1. Product Name: (CH3)(C6H5)C3N2(OH)C(O)C6H5
    2. Synonyms: (CH3)(C6H5)C3N2(OH)C(O)C6H5
    3. CAS NO:75898-02-1
    4. Molecular Formula:
    5. Molecular Weight: 278.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 75898-02-1.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: (CH3)(C6H5)C3N2(OH)C(O)C6H5(CAS DataBase Reference)
    10. NIST Chemistry Reference: (CH3)(C6H5)C3N2(OH)C(O)C6H5(75898-02-1)
    11. EPA Substance Registry System: (CH3)(C6H5)C3N2(OH)C(O)C6H5(75898-02-1)

  • 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: 75898-02-1(Hazardous Substances Data)

75898-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75898-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,9 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75898-02:
(7*7)+(6*5)+(5*8)+(4*9)+(3*8)+(2*0)+(1*2)=181
181 % 10 = 1
So 75898-02-1 is a valid CAS Registry Number.

75898-02-1Downstream Products

75898-02-1Relevant articles and documents

Regioselective synthesis of 1,3,5- and 1,3,4,5-substituted pyrazoles via acylation of N-Boc-N-substituted hydrazones

Tinarelli, Alessandro,Righi, Paolo,Rosini, Goffredo,Andreotti, Daniele,Profeta, Roberto,Spada, Simone

experimental part, p. 612 - 617 (2011/03/19)

Acylation of N-Boc-N-methylhydrazones followed by TFA treatment affords regioselective access to substituted pyrazoles. Both regioisomers of 1-methyl-3,5-disubstituted-1H-pyrazoles can be selectively obtained. This procedure can also be employed for the r

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