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

123458-71-9

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  • 123458-71-9 Structure
  • Basic information

    1. Product Name: 2-phenyl-3-benzylbenzothiophene
    2. Synonyms: 2-phenyl-3-benzylbenzothiophene
    3. CAS NO:123458-71-9
    4. Molecular Formula:
    5. Molecular Weight: 300.424
    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-phenyl-3-benzylbenzothiophene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-phenyl-3-benzylbenzothiophene(123458-71-9)
    11. EPA Substance Registry System: 2-phenyl-3-benzylbenzothiophene(123458-71-9)
  • 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: 123458-71-9(Hazardous Substances Data)

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123458-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123458-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,4,5 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 123458-71:
(8*1)+(7*2)+(6*3)+(5*4)+(4*5)+(3*8)+(2*7)+(1*1)=119
119 % 10 = 9
So 123458-71-9 is a valid CAS Registry Number.

123458-71-9Downstream Products

123458-71-9Relevant academic research and scientific papers

REACTION OF SULFUR WITH ORGANIC COMPOUNDS XXVI. REACTIONS OF SULUR WITH TOLUENE AND ITS EXO-SUBSTITUTED DERIVATIVES

Przewocki, K.,Voronkov, M. G.,Przewocka, L.,Varnke, Z.

, p. 2147 - 2154 (2007/10/02)

The reactions of sulfur with toluene and its exo-substituted derivatives of the PhCH2X type, where X = H, Cl, Br, I, OH, OCOMe, COOH, CH2Ph, SH, C(OH)(Ph)CH2Ph, and PhCH=Y, where Y = O, CHPh, C(Ph)CH2Ph, and also with 2-phenylbenzothiophene at 200 deg C and at the autogenous pressure were studied.In all cases the products of these reactions were bibenzyl, E- and Z-stilbenes, 2-phenylbenzothiophene, E- and Z-1,2,3-triphenylpropenes, 1,2,3-triphenylpropane, 2-phenyl-3-benzylbenzothiophene, tetraphenylthiophene, and pentaphenylcyclopentadiene, the ratios of whichare determined by the nature of the substituent X or Y.The high-molecular-weight reaction products with M 240 (34 compounds) were identified.

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