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1H-Indole, 6-nitro-3-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 94012-20-1 Structure
  • Basic information

    1. Product Name: 1H-Indole, 6-nitro-3-(phenylsulfonyl)-
    2. Synonyms:
    3. CAS NO:94012-20-1
    4. Molecular Formula: C14H10N2O4S
    5. Molecular Weight: 302.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 94012-20-1.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: 1H-Indole, 6-nitro-3-(phenylsulfonyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Indole, 6-nitro-3-(phenylsulfonyl)-(94012-20-1)
    11. EPA Substance Registry System: 1H-Indole, 6-nitro-3-(phenylsulfonyl)-(94012-20-1)
  • 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: 94012-20-1(Hazardous Substances Data)

94012-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94012-20-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,1 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 94012-20:
(7*9)+(6*4)+(5*0)+(4*1)+(3*2)+(2*2)+(1*0)=101
101 % 10 = 1
So 94012-20-1 is a valid CAS Registry Number.

94012-20-1Downstream Products

94012-20-1Relevant articles and documents

NEW SYNTHESIS OF SUBSTITUTED INDOLE DERIVATIVES VIA VICARIOUS NUCLEOPHILIC SUBSTITUTION OF HYDROGEN

Wojciechowski, K.,Makosza, M.

, p. 4793 - 4794 (2007/10/02)

Carbanions bearing leaving groups react with m-nitrophenyl isocyanides to form products of vicarious nucleophilic substitution of hydrogen which subsequently cyclize to corresponding indoles.

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