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2-nitro-3-N-benzylaminobenzothiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58763-85-2

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  • 58763-85-2 Structure
  • Basic information

    1. Product Name: 2-nitro-3-N-benzylaminobenzothiophene
    2. Synonyms: 2-nitro-3-N-benzylaminobenzothiophene
    3. CAS NO:58763-85-2
    4. Molecular Formula:
    5. Molecular Weight: 284.338
    6. EINECS: N/A
    7. Product Categories: N/A
  • 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-nitro-3-N-benzylaminobenzothiophene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-nitro-3-N-benzylaminobenzothiophene(58763-85-2)
    11. EPA Substance Registry System: 2-nitro-3-N-benzylaminobenzothiophene(58763-85-2)
  • 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: 58763-85-2(Hazardous Substances Data)

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58763-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58763-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,6 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58763-85:
(7*5)+(6*8)+(5*7)+(4*6)+(3*3)+(2*8)+(1*5)=172
172 % 10 = 2
So 58763-85-2 is a valid CAS Registry Number.

58763-85-2Relevant academic research and scientific papers

Synthesis of Substituted Benzothienopyrazines

Cannizzo, Sergio,Guerrera, Francesco,Siracusa, Maria Angela,Corsaro, Antonino

, p. 2175 - 2179 (2007/10/02)

The synthesis of a series of novel 1-unsubstituted and 1-alkyl-1,2,3,4-tetrahydrobenzothienopyrazine-2,3-diones 4a-d and their corresponding dialkylaminoalkylamino derivatives 6a-d starting from 2-nitro-3-bromobenzothiophene is described.The

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