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77486-54-5

5-Methyl-2-phenylsulfanyl-hex-4-enoic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 77486-54-5 Structure

  • Basic information

    1. Product Name: 5-Methyl-2-phenylsulfanyl-hex-4-enoic acid tert-butyl ester
    2. Synonyms: 5-Methyl-2-phenylsulfanyl-hex-4-enoic acid tert-butyl ester
    3. CAS NO:77486-54-5
    4. Molecular Formula:
    5. Molecular Weight: 292.442
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 77486-54-5.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: 5-Methyl-2-phenylsulfanyl-hex-4-enoic acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Methyl-2-phenylsulfanyl-hex-4-enoic acid tert-butyl ester(77486-54-5)
    11. EPA Substance Registry System: 5-Methyl-2-phenylsulfanyl-hex-4-enoic acid tert-butyl ester(77486-54-5)

  • 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: 77486-54-5(Hazardous Substances Data)

77486-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77486-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,8 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 77486-54:
(7*7)+(6*7)+(5*4)+(4*8)+(3*6)+(2*5)+(1*4)=175
175 % 10 = 5
So 77486-54-5 is a valid CAS Registry Number.

77486-54-5Downstream Products

77486-54-5Relevant articles and documents

REGIOSPECIFIC ALLYLATION OF SULFUR SUBSTITUTED ACTIVE METHYLENE COMPOUNDS WITH ALLYLIC BROMIDES

Ono, Noboru,Miyake, Hideyoshi,Tanabe, Yo,Tanaka, Kazuhiko,Kaji, Aritsune

, p. 1365 - 1368 (2007/10/02)

Allylation of sulfur substituted active methylene compounds such as RSCH2Y with allylic bromides in the presence of bases gives a mixture of the SN2-product and the apparent SN2'-product.The former product is selectively obtained in alkylation in a nonpolar solvent.Synthetic utility of this regiospecific allylation is demonstrated in the simple synthesis of pellitorine.

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