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<5-2H>-7-benzyl-3-formyl-6-phenylbenzothiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97679-40-8

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  • 97679-40-8 Structure

  • Basic information

    1. Product Name: <5-2H>-7-benzyl-3-formyl-6-phenylbenzothiophene
    2. Synonyms:
    3. CAS NO:97679-40-8
    4. Molecular Formula:
    5. Molecular Weight: 329.426
    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: <5-2H>-7-benzyl-3-formyl-6-phenylbenzothiophene(CAS DataBase Reference)
    10. NIST Chemistry Reference: <5-2H>-7-benzyl-3-formyl-6-phenylbenzothiophene(97679-40-8)
    11. EPA Substance Registry System: <5-2H>-7-benzyl-3-formyl-6-phenylbenzothiophene(97679-40-8)

  • 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: 97679-40-8(Hazardous Substances Data)

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97679-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97679-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,6,7 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 97679-40:
(7*9)+(6*7)+(5*6)+(4*7)+(3*9)+(2*4)+(1*0)=198
198 % 10 = 8
So 97679-40-8 is a valid CAS Registry Number.

97679-40-8Downstream Products

97679-40-8Relevant academic research and scientific papers

Cyclopropacycloheptathiophenones and Thiols: Unexpected Rearrangement with Dithiols leading to Benzo- and Cyclo-octa-thiophenes. Spectroscopic and Mechanistic Studies

Hanquet, Bernard,Guilard, Roger,Dusausoy, Yves

, p. 983 - 990 (2007/10/02)

Cyclopropacycloheptathiophen-5-one reacts in an acidic medium with thiols to give addition or rearrangement compounds: addition occurs with ethanethiol, but with 2-mercaptoethanol isomerization of the cyclopropyl ring to a vinyl group oc

UNUSUAL CARBON-CARBON DOUBLE BOND CLEAVAGE IN THIOPHENOHOMOTROPONE SYSTEM PROMOTED BY ETHANEDITHIOL

Hanquet, Bernard,Borai, Mohamed El,Guilard, Roger,Dusausoy, Yves

, p. 2859 - 2862 (2007/10/02)

Non classical carbon-carbon double bond cleavage in a homoaromatic system is initiated by ethanedithiol and p-toluenesulfonic acid.The structure of the unexpected product is proved by X-ray analysis.The proposed mechanism is supported by deuterium labelling experiments and common reactivity considerations.

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