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137777-73-2

1H-Indole, 3-(1,3-dithian-2-yl)-1-[(2-methylphenyl)sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 137777-73-2 Structure

  • Basic information

    1. Product Name: 1H-Indole, 3-(1,3-dithian-2-yl)-1-[(2-methylphenyl)sulfonyl]-
    2. Synonyms:
    3. CAS NO:137777-73-2
    4. Molecular Formula: C19H19NO2S3
    5. Molecular Weight: 389.563
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 137777-73-2.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, 3-(1,3-dithian-2-yl)-1-[(2-methylphenyl)sulfonyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Indole, 3-(1,3-dithian-2-yl)-1-[(2-methylphenyl)sulfonyl]-(137777-73-2)
    11. EPA Substance Registry System: 1H-Indole, 3-(1,3-dithian-2-yl)-1-[(2-methylphenyl)sulfonyl]-(137777-73-2)

  • 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: 137777-73-2(Hazardous Substances Data)

137777-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137777-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,7,7 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 137777-73:
(8*1)+(7*3)+(6*7)+(5*7)+(4*7)+(3*7)+(2*7)+(1*3)=172
172 % 10 = 2
So 137777-73-2 is a valid CAS Registry Number.

137777-73-2Downstream Products

137777-73-2Relevant articles and documents

Synthesis and reactivity of 2-(1,3-dithian-2-yl)indoles. IV. Influence of the N,N-deithylcarbamoyl indole protecting group

Castells,Troin,Diez,Rubiralta,Grierson,Husson

, p. 7911 - 7924 (2007/10/02)

The effect of the N,N-diethylcarbamoyl indole protecting group on the reactivity of 2-(1,3-dithian-2-yl)indole 7 in front of a series of electrophiles, as well as the potential synthetic usefulness of the resulting 2,2-disubstituted dithianes is reported.

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