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Hexadecanoic acid, 2-(acetyloxy)-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 95603-89-7 Structure
  • Basic information

    1. Product Name: Hexadecanoic acid, 2-(acetyloxy)-, (R)-
    2. Synonyms:
    3. CAS NO:95603-89-7
    4. Molecular Formula: C18H34O4
    5. Molecular Weight: 314.466
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 95603-89-7.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: Hexadecanoic acid, 2-(acetyloxy)-, (R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Hexadecanoic acid, 2-(acetyloxy)-, (R)-(95603-89-7)
    11. EPA Substance Registry System: Hexadecanoic acid, 2-(acetyloxy)-, (R)-(95603-89-7)
  • 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: 95603-89-7(Hazardous Substances Data)

95603-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95603-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,0 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 95603-89:
(7*9)+(6*5)+(5*6)+(4*0)+(3*3)+(2*8)+(1*9)=157
157 % 10 = 7
So 95603-89-7 is a valid CAS Registry Number.

95603-89-7Downstream Products

95603-89-7Relevant articles and documents

SYNTHESIS OF (4E,8E,2S,3R,2'R)-N-2'-HYDROXYHEXADECANOYL-9-METHYL-4,8-SPHINGADIENINE, THE CERAMIDE PORTION OF THE FRUITING-INDUCING CEREBROSIDE IN A BASIDIOMYCETE SCHIZOPHYLLUM COMMUNE, AND ITS (2R,3S)-ISOMER

Mori, Kenji,Funaki, Yuji

, p. 2369 - 2378 (2007/10/02)

A synthesis of the natural enantiomer as well as its diastereomer of the title compound was accomplished, confirming the structure proposed for the fruiting-inducing cerebroside of Schizophyllum commune.

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