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2-(o-Sulfinophenyl)-3-hydroxybenzothiophene 1,1-Dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74671-84-4

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  • 74671-84-4 Structure
  • Basic information

    1. Product Name: 2-(o-Sulfinophenyl)-3-hydroxybenzothiophene 1,1-Dioxide
    2. Synonyms: 2-(o-Sulfinophenyl)-3-hydroxybenzothiophene 1,1-Dioxide
    3. CAS NO:74671-84-4
    4. Molecular Formula:
    5. Molecular Weight: 322.362
    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-(o-Sulfinophenyl)-3-hydroxybenzothiophene 1,1-Dioxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(o-Sulfinophenyl)-3-hydroxybenzothiophene 1,1-Dioxide(74671-84-4)
    11. EPA Substance Registry System: 2-(o-Sulfinophenyl)-3-hydroxybenzothiophene 1,1-Dioxide(74671-84-4)
  • 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: 74671-84-4(Hazardous Substances Data)

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74671-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74671-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,7 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74671-84:
(7*7)+(6*4)+(5*6)+(4*7)+(3*1)+(2*8)+(1*4)=154
154 % 10 = 4
So 74671-84-4 is a valid CAS Registry Number.

74671-84-4Relevant academic research and scientific papers

NEW REACTION OF BENZOTHIENOBENZOTHIOPHENE DISULFONE

Udre, V.E.,Lukevits, E.Ya.,Kemme, A.A.,Bleidelis, Ya.Ya.

, p. 234 - 237 (2007/10/02)

A new reaction of benzothienobenzothiophene disulfone with amines that takes place with opening of one of the thiophene rings and nucleophilic substitution in the heteroaromatic ring at the site of cleavage of the S-C bond was observed.The mo

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