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2-methyl-1,3-diphenylbenzothiophenium bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106895-99-2

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  • 106895-99-2 Structure

  • Basic information

    1. Product Name: 2-methyl-1,3-diphenylbenzothiophenium bromide
    2. Synonyms: 2-methyl-1,3-diphenylbenzothiophenium bromide
    3. CAS NO:106895-99-2
    4. Molecular Formula:
    5. Molecular Weight: 381.336
    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-methyl-1,3-diphenylbenzothiophenium bromide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methyl-1,3-diphenylbenzothiophenium bromide(106895-99-2)
    11. EPA Substance Registry System: 2-methyl-1,3-diphenylbenzothiophenium bromide(106895-99-2)

  • 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: 106895-99-2(Hazardous Substances Data)

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106895-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106895-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,9 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 106895-99:
(8*1)+(7*0)+(6*6)+(5*8)+(4*9)+(3*5)+(2*9)+(1*9)=162
162 % 10 = 2
So 106895-99-2 is a valid CAS Registry Number.

106895-99-2Downstream Products

106895-99-2Relevant academic research and scientific papers

Intramolecular Cyclization of ethenes. Synthesis and Crystal Structure of 1-Arylbenzothiophenium Salts

Kitamura, Tsugio,Soda, Shin-ichi,Kawasato, Hironobu,Taniguchi, Hiroshi,Shiro, Motoo

, p. 5055 - 5066 (2007/10/02)

Novel 1-arylbenzothiophenium salts (4) are prepared by bromine-induced intramolecular cyclization of ethenes (3).The substituent and solvent effects on the formation of the 1-arylbenzothiophenium salts 4 are described.The reactio

FORMATION OF 1-ARYL-1-BENZOTHIOPHENIUM IONS IN BROMINATION OF o-ARYLTHIOPHENYL-SUBSTITUTED ETHYLENES

Kitamura, Tsugio,Kawasato, Hironobu,Kobayashi, Shinjiro,Taniguchi, Hiroshi

, p. 399 - 402 (2007/10/02)

Bromination reaction of o-arylthiophenyl-substituted ethylenes gave 1-aryl-1-benzothiophenium ions by intramolecular cyclization in the brominium intermediates.The substituent and solvent effects are also discussed.

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