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CAS

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363139-53-1

(R)-2-((2S,4S)-2-tert-Butyl-5-oxo-[1,3]dioxolan-4-yl)-3-(2,4,6-trimethyl-phenyl)-propionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 363139-53-1 Structure

  • Basic information

    1. Product Name: (R)-2-((2S,4S)-2-tert-Butyl-5-oxo-[1,3]dioxolan-4-yl)-3-(2,4,6-trimethyl-phenyl)-propionic acid
    2. Synonyms: (R)-2-((2S,4S)-2-tert-Butyl-5-oxo-[1,3]dioxolan-4-yl)-3-(2,4,6-trimethyl-phenyl)-propionic acid
    3. CAS NO:363139-53-1
    4. Molecular Formula:
    5. Molecular Weight: 334.412
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 363139-53-1.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: (R)-2-((2S,4S)-2-tert-Butyl-5-oxo-[1,3]dioxolan-4-yl)-3-(2,4,6-trimethyl-phenyl)-propionic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-((2S,4S)-2-tert-Butyl-5-oxo-[1,3]dioxolan-4-yl)-3-(2,4,6-trimethyl-phenyl)-propionic acid(363139-53-1)
    11. EPA Substance Registry System: (R)-2-((2S,4S)-2-tert-Butyl-5-oxo-[1,3]dioxolan-4-yl)-3-(2,4,6-trimethyl-phenyl)-propionic acid(363139-53-1)

  • 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: 363139-53-1(Hazardous Substances Data)

363139-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 363139-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,3,1,3 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 363139-53:
(8*3)+(7*6)+(6*3)+(5*1)+(4*3)+(3*9)+(2*5)+(1*3)=141
141 % 10 = 1
So 363139-53-1 is a valid CAS Registry Number.

363139-53-1Relevant articles and documents

Enantioselective synthesis of α-hydroxylated enterolactone and analogs

Sefkow, Michael,Kelling, Alexandra,Schilde, Uwe

, p. 5101 - 5104 (2007/10/03)

A short and general synthesis of enantiomerically pure α-hydroxylated lactone lignans starting from commercially available iPr malate is presented. Key reactions are two stereoselective alkylations of malic acid derivatives. Some enhancements of the alkylation of malic acid esters and a general extension of the alkylation of dioxolanones is reported. Proof of the stereochemical outcome of the alkylation reactions is provided by X-ray diffraction analysis of α-hydroxy-α,β-dibenzyl-γ-butyrolactone, the first crystal structure of an enantiomerically pure α-hydroxylated lactone lignan.

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