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121896-51-3

8-Benzyloxy-6-hydroxy-2-methyl-3-oxo-octanoic 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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  • 121896-51-3 Structure

  • Basic information

    1. Product Name: 8-Benzyloxy-6-hydroxy-2-methyl-3-oxo-octanoic acid methyl ester
    2. Synonyms:
    3. CAS NO:121896-51-3
    4. Molecular Formula:
    5. Molecular Weight: 308.375
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121896-51-3.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: 8-Benzyloxy-6-hydroxy-2-methyl-3-oxo-octanoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-Benzyloxy-6-hydroxy-2-methyl-3-oxo-octanoic acid methyl ester(121896-51-3)
    11. EPA Substance Registry System: 8-Benzyloxy-6-hydroxy-2-methyl-3-oxo-octanoic acid methyl ester(121896-51-3)

  • 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: 121896-51-3(Hazardous Substances Data)

121896-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121896-51-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,8,9 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 121896-51:
(8*1)+(7*2)+(6*1)+(5*8)+(4*9)+(3*6)+(2*5)+(1*1)=133
133 % 10 = 3
So 121896-51-3 is a valid CAS Registry Number.

121896-51-3Upstream product

121896-51-3Relevant articles and documents

STEREOSELECTIVE SYNTHESIS OF (+/-)-METHYL NONACTATE AND (+/-)-METHYL 8-epi-NONACTATE.

Lygo, Barry,O'Connor, Norval

, p. 3597 - 3600 (1987)

(+/-)-Methyl nonactate (2) and (+/-)-methyl 8epi-nonactate (3), synthetic precursors to the antibiotic nonactin have been synthesised, employing the reaction of substituted epoxides with dianions derived from β-ketoesters as the key carbon-carbon bond-for

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