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83541-10-0

(2S,4E)-2-methyl-2-phenyl-4-hexenoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83541-10-0 Structure

  • Basic information

    1. Product Name: (2S,4E)-2-methyl-2-phenyl-4-hexenoic acid
    2. Synonyms: (2S,4E)-2-methyl-2-phenyl-4-hexenoic acid
    3. CAS NO:83541-10-0
    4. Molecular Formula:
    5. Molecular Weight: 204.269
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83541-10-0.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: (2S,4E)-2-methyl-2-phenyl-4-hexenoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,4E)-2-methyl-2-phenyl-4-hexenoic acid(83541-10-0)
    11. EPA Substance Registry System: (2S,4E)-2-methyl-2-phenyl-4-hexenoic acid(83541-10-0)

  • 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: 83541-10-0(Hazardous Substances Data)

83541-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83541-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,4 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83541-10:
(7*8)+(6*3)+(5*5)+(4*4)+(3*1)+(2*1)+(1*0)=120
120 % 10 = 0
So 83541-10-0 is a valid CAS Registry Number.

83541-10-0Upstream product

83541-10-0Relevant articles and documents

Chemo- and Enantioselective Pd/B Hybrid Catalysis for the Construction of Acyclic Quaternary Carbons: Migratory Allylation of O-Allyl Esters to α- C-Allyl Carboxylic Acids

Fujita, Taiki,Yamamoto, Tomohiro,Morita, Yuya,Chen, Hongyu,Shimizu, Yohei,Kanai, Motomu

, p. 5899 - 5903 (2018)

We describe herein the asymmetric synthesis of α-allyl carboxylic acids containing an α-quaternary stereocenter by a chiral hybrid catalyst system comprising palladium and boron complexes. The reaction proceeded through palladium-catalyzed ionization of α,α-disubstituted O-allyl esters for the generation of chiral π-allyl palladium complex as an electrophile, boron-catalyzed enolization of the carboxylate part for the generation of chiral α,α-disubstituted carboxylic acid-derived enolates as a nucleophile, and enantioselective coupling between the thus-generated nucleophile and electrophile. Proper combinations of chiral ligands for the boron and palladium catalysts were crucial. The reaction proceeded chemoselectively at the α-position of the carboxylic acid group.

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