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CAS

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680622-02-0

8-Oxabicyclo[3.2.1]octane-2-carboxylicacid,(1S,2S,5S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 680622-02-0 Structure

  • Basic information

    1. Product Name: 8-Oxabicyclo[3.2.1]octane-2-carboxylicacid,(1S,2S,5S)-(9CI)
    2. Synonyms: 8-Oxabicyclo[3.2.1]octane-2-carboxylicacid,(1S,2S,5S)-(9CI)
    3. CAS NO:680622-02-0
    4. Molecular Formula: C8H12O3
    5. Molecular Weight: 156.18
    6. EINECS: N/A
    7. Product Categories: CARBOXYLICACID
    8. Mol File: 680622-02-0.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: 8-Oxabicyclo[3.2.1]octane-2-carboxylicacid,(1S,2S,5S)-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-Oxabicyclo[3.2.1]octane-2-carboxylicacid,(1S,2S,5S)-(9CI)(680622-02-0)
    11. EPA Substance Registry System: 8-Oxabicyclo[3.2.1]octane-2-carboxylicacid,(1S,2S,5S)-(9CI)(680622-02-0)

  • 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: 680622-02-0(Hazardous Substances Data)

680622-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 680622-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,0,6,2 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 680622-02:
(8*6)+(7*8)+(6*0)+(5*6)+(4*2)+(3*2)+(2*0)+(1*2)=150
150 % 10 = 0
So 680622-02-0 is a valid CAS Registry Number.

680622-02-0Upstream product

680622-02-0Downstream Products

680622-02-0Relevant articles and documents

A new nucleophilic addition/ring-closure sequence. Enantioselective synthesis of 3-deoxy-8-oxatropanes

Nguyen, Giang,Perlmutter, Patrick,Rose, Mark L.,Vounatsos, Filisaty

, p. 893 - 895 (2004)

(Equation presented) A study of new nucleophilic addition/ring-closure (NARC) sequences has resulted in the development of a stereoselective synthetic route to 3-deoxy-8-oxatropanes. The new sequences consisted of either a syn or anti aldol addition, empl

Bicylic type and method of preparing polycyclic mol.wt.

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Page 25-26, (2010/02/14)

The present application is directed to a method of synthesis of a bicyclic or polycyclic compound of formula I or formula II: in which E, G, Y, n, m, R, R1, R2, R3, R6, R7, R8 and R9

Process for preparation of bicyclic and polycyclic molecules

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Page 11, (2010/02/05)

A method of synthesis of a bicyclic or polycyclic compound of formula (I) or formula (II) in which: E represents an electrophile; each of R, R1, R2, R3, R6, R7, R8, R9 and X independently represents the common organic substituent groups defined in claim 1

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