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(1R,4S,6S)-7-oxabicyclo[2.2.1]heptane-6-carboxylic acid, also known as norbornane-6-carboxylic acid, is a unique chemical compound characterized by its bicyclic structure, featuring a fused 3-membered and 4-membered ring system. This carboxylic acid serves as a valuable building block in organic synthesis, particularly in the pharmaceutical industry.

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  • 38263-55-7 Structure
  • Basic information

    1. Product Name: (1R,4S,6S)-7-oxabicyclo[2.2.1]heptane-6-carboxylic acid
    2. Synonyms: (1R,4S,6S)-7-oxabicyclo[2.2.1]heptane-6-carboxylic acid
    3. CAS NO:38263-55-7
    4. Molecular Formula: C7H10O3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38263-55-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 290.7°C at 760 mmHg
    3. Flash Point: 125.8°C
    4. Appearance: /
    5. Density: 1.31g/cm3
    6. Vapor Pressure: 0.000508mmHg at 25°C
    7. Refractive Index: 1.528
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (1R,4S,6S)-7-oxabicyclo[2.2.1]heptane-6-carboxylic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: (1R,4S,6S)-7-oxabicyclo[2.2.1]heptane-6-carboxylic acid(38263-55-7)
    12. EPA Substance Registry System: (1R,4S,6S)-7-oxabicyclo[2.2.1]heptane-6-carboxylic acid(38263-55-7)
  • 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: 38263-55-7(Hazardous Substances Data)

38263-55-7 Usage

Uses

Used in Pharmaceutical Industry:
(1R,4S,6S)-7-oxabicyclo[2.2.1]heptane-6-carboxylic acid is utilized as a key building block in the development of novel drugs and pharmaceutical intermediates. Its specific stereochemistry and ring structure make it an attractive target for synthetic chemists and medicinal chemists, who aim to create new compounds with promising biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 38263-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,6 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38263-55:
(7*3)+(6*8)+(5*2)+(4*6)+(3*3)+(2*5)+(1*5)=127
127 % 10 = 7
So 38263-55-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O3/c8-7(9)5-3-4-1-2-6(5)10-4/h4-6H,1-3H2,(H,8,9)/t4-,5-,6+/m0/s1

38263-55-7Relevant articles and documents

The First Efficient Asymmetric Synthesis of 7-Oxabicyclohept-5-ene-2-carboxylate Derivatives

Takayama, Hiromitsu,Iyobe, Akira,Koizumi, Toru

, p. 771 - 772 (2007/10/02)

The asymmetric synthesis of 7-oxabicyclohept-5-ene-2-carboxylate derivatives was accomplished by the highly diastereoselective Diels-Alder reaction of (S)S- and (R)S-3-(2-pyridylsulphinyl)acrylates with furan.

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