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5-Benzyloxy-4-(3-hydroxy-phenyl)-3-oxo-pentanoic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 183799-11-3 Structure
  • Basic information

    1. Product Name: 5-Benzyloxy-4-(3-hydroxy-phenyl)-3-oxo-pentanoic acid ethyl ester
    2. Synonyms: 5-Benzyloxy-4-(3-hydroxy-phenyl)-3-oxo-pentanoic acid ethyl ester
    3. CAS NO:183799-11-3
    4. Molecular Formula:
    5. Molecular Weight: 342.392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 183799-11-3.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-Benzyloxy-4-(3-hydroxy-phenyl)-3-oxo-pentanoic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Benzyloxy-4-(3-hydroxy-phenyl)-3-oxo-pentanoic acid ethyl ester(183799-11-3)
    11. EPA Substance Registry System: 5-Benzyloxy-4-(3-hydroxy-phenyl)-3-oxo-pentanoic acid ethyl ester(183799-11-3)
  • 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: 183799-11-3(Hazardous Substances Data)

183799-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183799-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,7,9 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 183799-11:
(8*1)+(7*8)+(6*3)+(5*7)+(4*9)+(3*9)+(2*1)+(1*1)=183
183 % 10 = 3
So 183799-11-3 is a valid CAS Registry Number.

183799-11-3Upstream product

183799-11-3Relevant articles and documents

Enantio- and diastereoselective synthesis of the AB ring system of aklavinone by coupling a chemoenzymatic procedure with organometal chemistry

Banfi, Luca,Guanti, Giuseppe,Riva, Renata

, p. 13493 - 13512 (1996)

Two different approaches were investigated in order to prepare the title compound 2; best results were obtained when the tandem reduction/intramolecular hydroxyalkylation of the appropriate 5-alkoxy-(3-hydroxyphenyl)pentanoate was performed on an ester of chemoenzymatic origin, already bearing the two chiral centers present in 2 with the correct relative and absolute stereochemistry.

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