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1210348-12-1

(1R,3R,6S)-ethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate is a complex ester compound derived from a bicyclic structure with a seven-membered ring and a carboxylic acid group. It features three chiral centers, indicated by the 1R, 3R, and 6S configurations, allowing for multiple stereoisomeric forms. This molecule's intricate structure and chiral properties make it a candidate for applications in organic synthesis, medicinal chemistry, and other fields that necessitate specific stereochemistry.

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  • 1210348-12-1 Structure

  • Basic information

    1. Product Name: (1R,3R,6S)-ethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate
    2. Synonyms: (1R,3R,6S)-ethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate;(1R,3R,6S)-7-Oxabicyclo[4.1.0]heptane-3-carboxylic acid ethyl ester
    3. CAS NO:1210348-12-1
    4. Molecular Formula: C9H14O3
    5. Molecular Weight: 170.20566
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 1210348-12-1.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: (1R,3R,6S)-ethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,3R,6S)-ethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate(1210348-12-1)
    11. EPA Substance Registry System: (1R,3R,6S)-ethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate(1210348-12-1)

  • 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: 1210348-12-1(Hazardous Substances Data)

1210348-12-1 Usage

Uses

Used in Organic Synthesis:
(1R,3R,6S)-ethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate is used as a key intermediate in organic synthesis for the creation of complex molecules with specific stereochemistry. Its unique structure and chiral centers make it valuable for developing new compounds with tailored properties.
Used in Medicinal Chemistry:
In the pharmaceutical industry, (1R,3R,6S)-ethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate is used as a building block for the development of new drugs. Its specific stereochemistry can be leveraged to create molecules with targeted biological activities, potentially leading to more effective medications.
Used in Chiral Chemicals Production:
(1R,3R,6S)-ethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate is utilized as a precursor in the production of chiral chemicals. (1R,3R,6S)-ethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate's multiple stereoisomeric forms can be selectively synthesized to obtain enantiomerically pure products, which are essential in various chemical and pharmaceutical applications.
Used in Research and Development:
In academic and industrial research settings, (1R,3R,6S)-ethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate serves as a subject of study for understanding the properties and behavior of complex molecules with chiral centers. This knowledge can contribute to the advancement of synthetic methodologies and the discovery of novel applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1210348-12-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,0,3,4 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1210348-12:
(9*1)+(8*2)+(7*1)+(6*0)+(5*3)+(4*4)+(3*8)+(2*1)+(1*2)=91
91 % 10 = 1
So 1210348-12-1 is a valid CAS Registry Number.

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