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Thiophene, 2,5-dimethyl-3,4-bis(phenylmethyl)-, 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 178875-14-4 Structure
  • Basic information

    1. Product Name: Thiophene, 2,5-dimethyl-3,4-bis(phenylmethyl)-, 1-oxide
    2. Synonyms:
    3. CAS NO:178875-14-4
    4. Molecular Formula: C20H20OS
    5. Molecular Weight: 308.444
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 178875-14-4.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: Thiophene, 2,5-dimethyl-3,4-bis(phenylmethyl)-, 1-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: Thiophene, 2,5-dimethyl-3,4-bis(phenylmethyl)-, 1-oxide(178875-14-4)
    11. EPA Substance Registry System: Thiophene, 2,5-dimethyl-3,4-bis(phenylmethyl)-, 1-oxide(178875-14-4)
  • 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: 178875-14-4(Hazardous Substances Data)

178875-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 178875-14-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,8,7 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 178875-14:
(8*1)+(7*7)+(6*8)+(5*8)+(4*7)+(3*5)+(2*1)+(1*4)=194
194 % 10 = 4
So 178875-14-4 is a valid CAS Registry Number.

178875-14-4Relevant articles and documents

From thiophene S-oxides to 7-thiabicyclo[2.2.1]hept-5-enes

Li, Yuan-Qiang,Thiemann, Carolin,Ohira, Daisuke,Mataka, Shuntaro,Tashiro, Masashi,Thiemann, Thies

, p. 702 - 704 (2009)

Oligocycles with a 7-thiabicyclo[2.2.1]hept-5-ene unit have been prepared stereoselectively by cycloaddition of thiophene S-oxides to alkenes and subsequent deoxygenation of the sulfoxy bridge of the cycloadducts with PBr 3.

Lewis Acid Catalysis in the Oxidative Cycloaddition of Thiophenes

Li, Yuanqiang,Thiemann, Thies,Sawada, Tsuyoshi,Mataka, Shuntaro,Tashiro, Masashi

, p. 7926 - 7936 (1997)

Thiophenes 1 were treated with m-chloroperbenzoic acid (m-CPBA) under BF3·Et2D catalysis to afford thiophene S-monoxides. These could be reacted in situ as intermediary species with a number of dienophiles to provide arenes (with alk

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