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60010-74-4

desmodilactone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 60010-74-4 Structure

  • Basic information

    1. Product Name: desmodilactone
    2. Synonyms: desmodilactone
    3. CAS NO:60010-74-4
    4. Molecular Formula: C8H13NO3
    5. Molecular Weight: 171.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 60010-74-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 402.8°C at 760 mmHg
    3. Flash Point: 197.4°C
    4. Appearance: /
    5. Density: 1.12g/cm3
    6. Vapor Pressure: 1.07E-06mmHg at 25°C
    7. Refractive Index: 1.47
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: desmodilactone(CAS DataBase Reference)
    11. NIST Chemistry Reference: desmodilactone(60010-74-4)
    12. EPA Substance Registry System: desmodilactone(60010-74-4)

  • 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: 60010-74-4(Hazardous Substances Data)

60010-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60010-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,1 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60010-74:
(7*6)+(6*0)+(5*0)+(4*1)+(3*0)+(2*7)+(1*4)=64
64 % 10 = 4
So 60010-74-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO3/c1-4-5(2)12-8(11)7(4)9-6(3)10/h4-5,7H,1-3H3,(H,9,10)/t4-,5+,7+/m0/s1

60010-74-4Upstream product

60010-74-4Downstream Products

60010-74-4Relevant articles and documents

Method for preparing 4-hydroxyisoleucine diastereoisomers and enantiomers and derivatives thereof

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Page/Page column 8, (2010/11/23)

The invention concerns a method for preparing 4-hydroxyisoleucine diastereoisomers and enantiomers and derivatives thereof of general formula (I), characterized in that it consists in reducing an isoxazole derivative of formula (II) in conditions directly

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