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(S)-1-adamantanyl 2-hydroxy-1-oxo-1,2,3,4-tetrahydro-naphthalene-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (S)-1-adamantanyl 2-hydroxy-1-oxo-1,2,3,4-tetrahydro-naphthalene-2-carboxylate

    Cas No: 923569-26-0

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  • 923569-26-0 Structure
  • Basic information

    1. Product Name: (S)-1-adamantanyl 2-hydroxy-1-oxo-1,2,3,4-tetrahydro-naphthalene-2-carboxylate
    2. Synonyms:
    3. CAS NO:923569-26-0
    4. Molecular Formula:
    5. Molecular Weight: 340.419
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 923569-26-0.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: (S)-1-adamantanyl 2-hydroxy-1-oxo-1,2,3,4-tetrahydro-naphthalene-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-1-adamantanyl 2-hydroxy-1-oxo-1,2,3,4-tetrahydro-naphthalene-2-carboxylate(923569-26-0)
    11. EPA Substance Registry System: (S)-1-adamantanyl 2-hydroxy-1-oxo-1,2,3,4-tetrahydro-naphthalene-2-carboxylate(923569-26-0)
  • 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: 923569-26-0(Hazardous Substances Data)

923569-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 923569-26-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,5,6 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 923569-26:
(8*9)+(7*2)+(6*3)+(5*5)+(4*6)+(3*9)+(2*2)+(1*6)=190
190 % 10 = 0
So 923569-26-0 is a valid CAS Registry Number.

923569-26-0Upstream product

923569-26-0Downstream Products

923569-26-0Relevant articles and documents

Enantioselective α-Benzoyloxylation of β-Keto Esters by N-Oxide Phase-Transfer Catalysts

Wang, Yakun,Gao, Qinghe,Liu, Zhaomin,Bai, Suping,Tang, Xiaofei,Yin, Hang,Meng, Qingwei

, p. 2263 - 2273 (2018)

An efficient and enantioselective α-benzoyloxylation of β-keto esters has been achieved by phase-transfer catalysis. This simple catalytic procedure is applicable to a range of β-keto esters with cinchona-derived N-oxide asymmetric phase-transfer catalysts and gives the corresponding products in good enantiopurity (up to 95% ee) and yield (up to 99%). This simple and effective oxyfunctionalization is a useful synthetic strategy for introducing an oxygen-containing functional group at the α position of β-dicarbonyl compounds.

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