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171815-24-0

ethyl 4,5-dihydro-4-(phenylmethoxy)-3-isoxazolecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 171815-24-0 Structure

  • Basic information

    1. Product Name: ethyl 4,5-dihydro-4-(phenylmethoxy)-3-isoxazolecarboxylate
    2. Synonyms: ethyl 4,5-dihydro-4-(phenylmethoxy)-3-isoxazolecarboxylate
    3. CAS NO:171815-24-0
    4. Molecular Formula:
    5. Molecular Weight: 249.266
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 171815-24-0.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: ethyl 4,5-dihydro-4-(phenylmethoxy)-3-isoxazolecarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 4,5-dihydro-4-(phenylmethoxy)-3-isoxazolecarboxylate(171815-24-0)
    11. EPA Substance Registry System: ethyl 4,5-dihydro-4-(phenylmethoxy)-3-isoxazolecarboxylate(171815-24-0)

  • 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: 171815-24-0(Hazardous Substances Data)

171815-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 171815-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,8,1 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 171815-24:
(8*1)+(7*7)+(6*1)+(5*8)+(4*1)+(3*5)+(2*2)+(1*4)=130
130 % 10 = 0
So 171815-24-0 is a valid CAS Registry Number.

171815-24-0Relevant articles and documents

2-Amino-2-deoxytetrose derivatives. Preparation from 4,5-dihydroisoxazoles via reductive cleavage

Wade,D'Ambrosio,Price

, p. 6302 - 6308 (2007/10/03)

The 4-alkoxy-3-nitro-4,5-dihydroisoxazoles 2a,b were prepared by condensation of nitromethane and chloroacetaldehyde, protection of the resulting nitroaldol 1c, and subsequent nitrosative cyclization. Multistep replacement of the nitrogroup of 2a,b by a 2

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