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

111359-33-2

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  • 111359-33-2 Structure

  • Basic information

    1. Product Name: 2-dimethylamino-3-phenylbenzothiophene
    2. Synonyms: 2-dimethylamino-3-phenylbenzothiophene
    3. CAS NO:111359-33-2
    4. Molecular Formula:
    5. Molecular Weight: 253.368
    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-dimethylamino-3-phenylbenzothiophene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-dimethylamino-3-phenylbenzothiophene(111359-33-2)
    11. EPA Substance Registry System: 2-dimethylamino-3-phenylbenzothiophene(111359-33-2)

  • 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: 111359-33-2(Hazardous Substances Data)

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111359-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111359-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,3,5 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 111359-33:
(8*1)+(7*1)+(6*1)+(5*3)+(4*5)+(3*9)+(2*3)+(1*3)=92
92 % 10 = 2
So 111359-33-2 is a valid CAS Registry Number.

111359-33-2Downstream Products

111359-33-2Relevant academic research and scientific papers

DESTABILIZED CARBOCATIONS. NUCLEAR MATNETIC RESONANCE DETECTION AND REACTIVITIES OF ARYL α-THIOFORMAMIDYL CATIONS

Ablenas, F. J.,George, B. E.,Maleki, M.,Jain, R.,Hopkinson, A. C.,Lee-Ruff, E.

, p. 1800 - 1803 (2007/10/02)

A series of α-aryl and diarylthioformamidyl cations were observed by low-temperature nuclear magnetic resonance spectroscopy.These ions undergo efficient cyclization and deprotonation to give benzothiophenes.

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