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217435-90-0

3-(3-Ethyl-5-methoxy-tetrahydro-furan-3-yl)-propionic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 217435-90-0 Structure

  • Basic information

    1. Product Name: 3-(3-Ethyl-5-methoxy-tetrahydro-furan-3-yl)-propionic acid methyl ester
    2. Synonyms:
    3. CAS NO:217435-90-0
    4. Molecular Formula:
    5. Molecular Weight: 216.277
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 217435-90-0.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: 3-(3-Ethyl-5-methoxy-tetrahydro-furan-3-yl)-propionic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(3-Ethyl-5-methoxy-tetrahydro-furan-3-yl)-propionic acid methyl ester(217435-90-0)
    11. EPA Substance Registry System: 3-(3-Ethyl-5-methoxy-tetrahydro-furan-3-yl)-propionic acid methyl ester(217435-90-0)

  • 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: 217435-90-0(Hazardous Substances Data)

217435-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 217435-90-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,4,3 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 217435-90:
(8*2)+(7*1)+(6*7)+(5*4)+(4*3)+(3*5)+(2*9)+(1*0)=130
130 % 10 = 0
So 217435-90-0 is a valid CAS Registry Number.

217435-90-0Relevant articles and documents

An efficient synthesis of 4-ethyl-4-[(3-hydroxycarbonyl)propyl]dihydro- 2(3h)-furanone and its use in a formal total synthesis of (±)-quebrachamine

Wee, Andrew G. H.,Yu, Qing

, p. 13435 - 13448 (1998)

The Rh2(OAch)4-catalyzed reaction of diazoacetate 5 provides ready access to the pivotal cyclic acetal 13 that undergoes Pictet-Spengler-type condensation with tryptamine to directly afford an epimeric mixture of the tetracyclic lactam 17a,b. Lithium aluminum hydride reduction of 17a,b provides the known tetracyclic amino alcohol 18a,b which, overall, constitutes a formal synthesis of (±)-quebrachamine.

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