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(1R, 2S, 3R, 4R)-4-benzoyloxy-2-(dimethoxymethyl)-3-methyl-1-cyclopentaneacetic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108377-15-7 Structure
  • Basic information

    1. Product Name: (1R, 2S, 3R, 4R)-4-benzoyloxy-2-(dimethoxymethyl)-3-methyl-1-cyclopentaneacetic acid methyl ester
    2. Synonyms: (1R, 2S, 3R, 4R)-4-benzoyloxy-2-(dimethoxymethyl)-3-methyl-1-cyclopentaneacetic acid methyl ester
    3. CAS NO:108377-15-7
    4. Molecular Formula:
    5. Molecular Weight: 350.412
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108377-15-7.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: (1R, 2S, 3R, 4R)-4-benzoyloxy-2-(dimethoxymethyl)-3-methyl-1-cyclopentaneacetic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R, 2S, 3R, 4R)-4-benzoyloxy-2-(dimethoxymethyl)-3-methyl-1-cyclopentaneacetic acid methyl ester(108377-15-7)
    11. EPA Substance Registry System: (1R, 2S, 3R, 4R)-4-benzoyloxy-2-(dimethoxymethyl)-3-methyl-1-cyclopentaneacetic acid methyl ester(108377-15-7)
  • 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: 108377-15-7(Hazardous Substances Data)

108377-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108377-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,7 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 108377-15:
(8*1)+(7*0)+(6*8)+(5*3)+(4*7)+(3*7)+(2*1)+(1*5)=127
127 % 10 = 7
So 108377-15-7 is a valid CAS Registry Number.

108377-15-7Relevant articles and documents

IRIDOIDS : ENANTIOSELECTIVE SYNTHESIS OF LOGANIN VIA AN ASYMMETRIC DIELS-ALDER REACTION

Vandewalle, M.,Van der Eycken, J.,Oppolzer, W.,Vullioud, C.

, p. 4035 - 4044 (1986)

Starting from (-)-camphor-10-sulfonic acid (5) the crystalline sultam 9 was readily prepared.TiCl4-mediated Diels-Alder addition of the N-crotonyl sultam 11 to cyclopentadiene, crystallization of the resulrting adduct 12 and subsequent reduction gave virtually pure (1S, 4R,5R, 6S)-1 together with recovered auxiliary 9.The loganin precursor 1 was transformed into norbonanone 20, which upon Baeyer-Villiger oxidation led to the suitably substituted cyclopentane 22 from which 1-B-O-methyl loganin aglucone (2) was readily available.

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