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CAS

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131543-60-7

(3aR,4R,5R,6aS)-5-(benzoyloxy)hexahydro-4-(iodomethyl)-2H-cyclopentafuran-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131543-60-7 Structure

  • Basic information

    1. Product Name: (3aR,4R,5R,6aS)-5-(benzoyloxy)hexahydro-4-(iodomethyl)-2H-cyclopentafuran-2-one
    2. Synonyms: (3aR,4R,5R,6aS)-5-(benzoyloxy)hexahydro-4-(iodomethyl)-2H-cyclopentafuran-2-one
    3. CAS NO:131543-60-7
    4. Molecular Formula:
    5. Molecular Weight: 386.186
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131543-60-7.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: (3aR,4R,5R,6aS)-5-(benzoyloxy)hexahydro-4-(iodomethyl)-2H-cyclopentafuran-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3aR,4R,5R,6aS)-5-(benzoyloxy)hexahydro-4-(iodomethyl)-2H-cyclopentafuran-2-one(131543-60-7)
    11. EPA Substance Registry System: (3aR,4R,5R,6aS)-5-(benzoyloxy)hexahydro-4-(iodomethyl)-2H-cyclopentafuran-2-one(131543-60-7)

  • 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: 131543-60-7(Hazardous Substances Data)

131543-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131543-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,5,4 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 131543-60:
(8*1)+(7*3)+(6*1)+(5*5)+(4*4)+(3*3)+(2*6)+(1*0)=97
97 % 10 = 7
So 131543-60-7 is a valid CAS Registry Number.

131543-60-7Relevant articles and documents

Stereoselective preparation of key intermediates for the synthesis of iso-, neuro- and phyto-prostane family members: Inaugural asymmetric synthesis of 17-E2c-dihomo- and 17-F2c-dihomo-isoprostanes

Gandini, Andrea,Amin, Ahmed A.,Amin, Hawraz Ibrahim M.,Corriero, Davide,Porta, Alessio,Zanoni, Giuseppe

supporting information, p. 2393 - 2396 (2018/04/12)

A practical methodology for the synthesis of key intermediates for isoprostane, neuroprostane and dihomo-isoprostane preparation has been described. The key strategy involved a three stage C-12 stereocenter inversion of the configuration of a Corey lacton

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