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132439-88-4

3H,6H-Furo[3,4-c]isoxazole,3a,4-dihydro-6-(1-methylethyl)-,trans-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 3H,6H-Furo[3,4-c]isoxazole,3a,4-dihydro-6-(1-methylethyl)-,trans-(9CI)

    Cas No: 132439-88-4

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  • 132439-88-4 Structure

  • Basic information

    1. Product Name: 3H,6H-Furo[3,4-c]isoxazole,3a,4-dihydro-6-(1-methylethyl)-,trans-(9CI)
    2. Synonyms: 3H,6H-Furo[3,4-c]isoxazole,3a,4-dihydro-6-(1-methylethyl)-,trans-(9CI)
    3. CAS NO:132439-88-4
    4. Molecular Formula: C8H13NO2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: ISOPROPYL
    8. Mol File: 132439-88-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3H,6H-Furo[3,4-c]isoxazole,3a,4-dihydro-6-(1-methylethyl)-,trans-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3H,6H-Furo[3,4-c]isoxazole,3a,4-dihydro-6-(1-methylethyl)-,trans-(9CI)(132439-88-4)
    11. EPA Substance Registry System: 3H,6H-Furo[3,4-c]isoxazole,3a,4-dihydro-6-(1-methylethyl)-,trans-(9CI)(132439-88-4)

  • 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: 132439-88-4(Hazardous Substances Data)

132439-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132439-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,3 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132439-88:
(8*1)+(7*3)+(6*2)+(5*4)+(4*3)+(3*9)+(2*8)+(1*8)=124
124 % 10 = 4
So 132439-88-4 is a valid CAS Registry Number.

132439-88-4Downstream Products

132439-88-4Relevant articles and documents

A Route to Functionalized Cyclic Ethers by Intramolecular Cycloaddition of Unsaturated Nitro Ethers

Hassner, Alfred,Dehaen, Wim

, p. 1181 - 1186 (2007/10/02)

A convenient conversion of aldehydes via nitroolefins 2 into cyclic ethers 6 fused to an isoxazoline ring involves formation of unsaturated nitroalkyl ethers 4 and subsequent intramolecular cycloaddition of an in situ-formed nitrile oxide olefin.The cyclization proceeds with stereoselective formation of trans over cis isomers in the tetrahydrofuran series and opposite stereoselectivity in the tetrahydropyran and hexahydrooxepine series, depending on the substituent R in the original nitro compound, thus providing access to stereoselectively functionalized cyclic ethers.

Double diastereoselectivity in the intramolecular nitrile oxide-olefin cycloaddition (INOC) reaction

Kim, Hyoung Rae,Kim, Hyung Jin,Duffy, Jetty L.,Olmstead, Marilyn M.,Ruhlandt-Senge, Karin,Kurth, Mark J.

, p. 4259 - 4262 (2007/10/02)

An investigation of relative asymmetric induction and double diastereoselectivity in the intramolecular nitrile oxide-olefin cycloaddition (INOC) reaction is presented.

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