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

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  • 137777-71-0 Structure
  • Basic information

    1. Product Name: 1H-Indole, 3-(1,3-dithian-2-yl)-1-(phenylsulfonyl)-
    2. Synonyms:
    3. CAS NO:137777-71-0
    4. Molecular Formula: C18H17NO2S3
    5. Molecular Weight: 375.536
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 137777-71-0.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-(phenylsulfonyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Indole, 3-(1,3-dithian-2-yl)-1-(phenylsulfonyl)-(137777-71-0)
    11. EPA Substance Registry System: 1H-Indole, 3-(1,3-dithian-2-yl)-1-(phenylsulfonyl)-(137777-71-0)
  • 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: 137777-71-0(Hazardous Substances Data)

137777-71-0 Usage

Molecular structure

1H-Indole core with attached 1,3-dithian-2-yl and phenylsulfonyl groups.

Aromatic properties

The 1H-indole core provides basic aromatic characteristics to the molecule.

Reactivity

The 1,3-dithian-2-yl and phenylsulfonyl groups contribute to the molecule's specific reactivity.

Functionality

The presence of the 1,3-dithian-2-yl and phenylsulfonyl groups adds unique functional groups to the molecule.

Usage in organic synthesis

Commonly used in organic synthesis due to its versatile chemical properties.

Pharmaceutical research

Has potential applications in the development of pharmaceuticals.

Agrochemical development

Can be utilized in the creation of agrochemicals.

Unique structural features

The combination of the 1H-indole core and the attached groups results in a distinctive molecular structure.

Check Digit Verification of cas no

The CAS Registry Mumber 137777-71-0 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 137777-71:
(8*1)+(7*3)+(6*7)+(5*7)+(4*7)+(3*7)+(2*7)+(1*1)=170
170 % 10 = 0
So 137777-71-0 is a valid CAS Registry Number.

137777-71-0Relevant 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 (1991)

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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