Welcome to LookChem.com Sign In|Join Free

CAS

  • or

78840-03-6

Benzene, [3-(ethylthio)-1-methyl-1-butenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78840-03-6 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 78840-03-6 Structure

  • Basic information

    1. Product Name: Benzene, [3-(ethylthio)-1-methyl-1-butenyl]-
    2. Synonyms:
    3. CAS NO:78840-03-6
    4. Molecular Formula: C13H18S
    5. Molecular Weight: 206.352
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78840-03-6.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: Benzene, [3-(ethylthio)-1-methyl-1-butenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, [3-(ethylthio)-1-methyl-1-butenyl]-(78840-03-6)
    11. EPA Substance Registry System: Benzene, [3-(ethylthio)-1-methyl-1-butenyl]-(78840-03-6)

  • 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: 78840-03-6(Hazardous Substances Data)

78840-03-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78840-03-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,4 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78840-03:
(7*7)+(6*8)+(5*8)+(4*4)+(3*0)+(2*0)+(1*3)=156
156 % 10 = 6
So 78840-03-6 is a valid CAS Registry Number.

78840-03-6Downstream Products

78840-03-6Relevant articles and documents

CROSS-COUPLING REACTION BETWEEN ENOL PHOSPHATES AND ORGANOALUMINIUM COMPOUNDS IN THE PRESENCE OF PALLADIUM(0) CATALYST.

Takai,Sato,Oshima,Nozaki

, p. 108 - 115 (2007/10/02)

The title reaction in the presence of a catalytic amount of tetrakis(triphenylphosphine)palladium(0) affords alkylative coupling products in good to excellent yields in 1,2-dichloroethane at room temperature. This coupling reaction under C(sp**2)-O cleavage proceeds stereospecifically. The reaction does not affect a coexisting vinyl sulfide group. This feature enables 1,2- and 1,3-carbonyl transposition with or without alkylation via phenylthio-substituted enol phosphates.

Pd(O) PROMOTED ALKYLATION OF ENOL PHOSPHATES WITH ORGANOALUMINIUM COMPOUNDS AND ITS SYNTHETIC APPLICATIONS

Sato, Mitsuyoshi,Takai, Kazuhiko,Oshima, Koichiro,Nozaki, Hitosi

, p. 1609 - 1612 (2007/10/02)

Keto carbonyl 1,2- and 1,3-transpositions with and without alkylation of the substrate are described together with ketone synthesis from thiocarboxylic S-ester.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 78840-03-6