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CAS

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1361325-67-8

methyl 4-((1R,5R,7R)-5-isopropyl-2-methyl-6-oxabicyclo[3.2.1]oct-2-en-7-yl)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1361325-67-8 Structure

  • Basic information

    1. Product Name: methyl 4-((1R,5R,7R)-5-isopropyl-2-methyl-6-oxabicyclo[3.2.1]oct-2-en-7-yl)benzoate
    2. Synonyms: methyl 4-((1R,5R,7R)-5-isopropyl-2-methyl-6-oxabicyclo[3.2.1]oct-2-en-7-yl)benzoate
    3. CAS NO:1361325-67-8
    4. Molecular Formula:
    5. Molecular Weight: 300.398
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1361325-67-8.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: methyl 4-((1R,5R,7R)-5-isopropyl-2-methyl-6-oxabicyclo[3.2.1]oct-2-en-7-yl)benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 4-((1R,5R,7R)-5-isopropyl-2-methyl-6-oxabicyclo[3.2.1]oct-2-en-7-yl)benzoate(1361325-67-8)
    11. EPA Substance Registry System: methyl 4-((1R,5R,7R)-5-isopropyl-2-methyl-6-oxabicyclo[3.2.1]oct-2-en-7-yl)benzoate(1361325-67-8)

  • 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: 1361325-67-8(Hazardous Substances Data)

1361325-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1361325-67-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,3,2 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1361325-67:
(9*1)+(8*3)+(7*6)+(6*1)+(5*3)+(4*2)+(3*5)+(2*6)+(1*7)=138
138 % 10 = 8
So 1361325-67-8 is a valid CAS Registry Number.

1361325-67-8Downstream Products

1361325-67-8Relevant articles and documents

Stereoselective synthesis of 6-oxabicyclo[3.2.1]octene via (3,5)-oxonium-ene reaction

Saha, Pipas,Saikia, Anil K.

experimental part, p. 2261 - 2266 (2012/04/11)

Oxabicyclo[3.2.1]octene can efficiently be synthesized by the reaction of (-)-terpinen-4-ol and aldehyde or epoxide catalyzed by indium triflate (In(OTf)3) in good yields. The reaction is stereoselective and proceeds via (3,5)-oxonium-ene-type

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