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141936-22-3

6-Bromo-6-demethylmitomycin C is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141936-22-3 Structure

  • Basic information

    1. Product Name: 6-Bromo-6-demethylmitomycin C
    2. Synonyms:
    3. CAS NO:141936-22-3
    4. Molecular Formula:
    5. Molecular Weight: 399.201
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141936-22-3.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: 6-Bromo-6-demethylmitomycin C(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Bromo-6-demethylmitomycin C(141936-22-3)
    11. EPA Substance Registry System: 6-Bromo-6-demethylmitomycin C(141936-22-3)

  • 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: 141936-22-3(Hazardous Substances Data)

141936-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141936-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,9,3 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 141936-22:
(8*1)+(7*4)+(6*1)+(5*9)+(4*3)+(3*6)+(2*2)+(1*2)=123
123 % 10 = 3
So 141936-22-3 is a valid CAS Registry Number.

141936-22-3Upstream product

141936-22-3Downstream Products

141936-22-3Relevant articles and documents

6-Demethyl-6-halo- and 6-Demethyl-6-thiomitomycins: Synthesis of Novel Mitomycin Derivatives Involving a Tandem Michael Addition/Retro-Mannich Reaction Sequence

Arai, Hitoshi,Kasai, Masaji

, p. 1087 - 1094 (1994)

Synthesis of novel 6-demethyl-6-halomitomycins (3, 4, 6, and 7) and 6-demethyl-6-thiomytomycins (5 and 8) is described from key intermediates, namely, 6-demethyl-7,7-(ethylenedioxy)-6,6-dihalo-6,7-dihydromitosanes (18 and 19) and 6-demethyl-7,7-(ethylenedioxy)-6,7-dihydro-6-thiomitosane (20), respectively.Compounds 18-20 were prepared through a tandem Michael addition and a retro-Mannich reaction sequence (N-halosucinimide or cationic arylsulfenyl species in the presence of Et2NH) on 10.

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