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183116-89-4

(R)-4-Benzhydryl-3-hexadecanoyl-oxazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 183116-89-4 Structure

  • Basic information

    1. Product Name: (R)-4-Benzhydryl-3-hexadecanoyl-oxazolidin-2-one
    2. Synonyms:
    3. CAS NO:183116-89-4
    4. Molecular Formula:
    5. Molecular Weight: 491.714
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 183116-89-4.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)-4-Benzhydryl-3-hexadecanoyl-oxazolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-4-Benzhydryl-3-hexadecanoyl-oxazolidin-2-one(183116-89-4)
    11. EPA Substance Registry System: (R)-4-Benzhydryl-3-hexadecanoyl-oxazolidin-2-one(183116-89-4)

  • 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: 183116-89-4(Hazardous Substances Data)

183116-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183116-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,1,1 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 183116-89:
(8*1)+(7*8)+(6*3)+(5*1)+(4*1)+(3*6)+(2*8)+(1*9)=134
134 % 10 = 4
So 183116-89-4 is a valid CAS Registry Number.

183116-89-4Relevant articles and documents

Enantiospecific synthesis of trisubstituted butyrolactone natural products and their analogs

Sibi, Mukund P.,Lu, Jianliang,Talbacka, Chelsy L.

, p. 7848 - 7855 (1996)

A general methodology for the synthesis of highly substituted butyrolactones in enantiomerically pure form has been developed. The application of this process in a highly efficient synthesis of lactone natural products blastmycinone (1), NFX-2 (2), antimycinone (3), and NFX-4 (4) and two lipid metabolites (5, 6) are described. Additionally, the total synthesis of 5-epi-blastmycinone (22), 5-epi-NFX-2 (21b), 5-epi-NFX-4 (21c), and lipid metabolite analogs (19, 20) are also described. The overall yields for the target molecules are the highest reported so far in the literature.

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