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(2R,5S)-2,5-dimethyl-2-ethyl-5-hydroxypentanoic acid lactone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103712-18-1 Structure
  • Basic information

    1. Product Name: (2R,5S)-2,5-dimethyl-2-ethyl-5-hydroxypentanoic acid lactone
    2. Synonyms:
    3. CAS NO:103712-18-1
    4. Molecular Formula:
    5. Molecular Weight: 156.225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103712-18-1.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: (2R,5S)-2,5-dimethyl-2-ethyl-5-hydroxypentanoic acid lactone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,5S)-2,5-dimethyl-2-ethyl-5-hydroxypentanoic acid lactone(103712-18-1)
    11. EPA Substance Registry System: (2R,5S)-2,5-dimethyl-2-ethyl-5-hydroxypentanoic acid lactone(103712-18-1)
  • 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: 103712-18-1(Hazardous Substances Data)

103712-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103712-18-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,1 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 103712-18:
(8*1)+(7*0)+(6*3)+(5*7)+(4*1)+(3*2)+(2*1)+(1*8)=81
81 % 10 = 1
So 103712-18-1 is a valid CAS Registry Number.

103712-18-1Downstream Products

103712-18-1Relevant articles and documents

Degradation and Absolute Configurational Assignment to C34-Botryococcene

White, James D.,Somers, Todd C.,Reddy, G. Nagabushana

, p. 4991 - 4998 (1992)

C34-Botryococcene, the major hydrocarbon constituent of the B race of Botryococcus braunii, was degraded by ozonolysis of its dihydro derivative followed by Baeyer-Villiger oxidation to γ-valerolactone, 2,5-dimethylhexanolactone, and 2-ethyl-2,

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