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CAS

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227002-09-7

6-Oxabicyclo[3.2.1]oct-2-en-7-one, 4-(benzoyloxy)-1-hydroxy-, (1R,4R,5R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 227002-09-7 Structure

  • Basic information

    1. Product Name: 6-Oxabicyclo[3.2.1]oct-2-en-7-one, 4-(benzoyloxy)-1-hydroxy-, (1R,4R,5R)-
    2. Synonyms:
    3. CAS NO:227002-09-7
    4. Molecular Formula: C14H12O5
    5. Molecular Weight: 260.246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 227002-09-7.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: 6-Oxabicyclo[3.2.1]oct-2-en-7-one, 4-(benzoyloxy)-1-hydroxy-, (1R,4R,5R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Oxabicyclo[3.2.1]oct-2-en-7-one, 4-(benzoyloxy)-1-hydroxy-, (1R,4R,5R)-(227002-09-7)
    11. EPA Substance Registry System: 6-Oxabicyclo[3.2.1]oct-2-en-7-one, 4-(benzoyloxy)-1-hydroxy-, (1R,4R,5R)-(227002-09-7)

  • 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: 227002-09-7(Hazardous Substances Data)

227002-09-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 227002-09-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,7,0,0 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 227002-09:
(8*2)+(7*2)+(6*7)+(5*0)+(4*0)+(3*2)+(2*0)+(1*9)=87
87 % 10 = 7
So 227002-09-7 is a valid CAS Registry Number.

227002-09-7Relevant articles and documents

Synthesis of carba-sugars from (-)-quinic acid

Carballido, Montserrat,Castedo, Luis,González, Concepción

, p. 3973 - 3976 (2001)

(1S,2R,3R,4S,5R)- (3a) and (1S,2S,3S,4S,5R)-1,2,3,4,5-pentahydroxy-1-hydroxymethylcyclohexane (4a), (1R,2R,3R,4S,5R)- (3b) and (1R,2S,3S,4S,5R)-1,2,3,4,5-pentahydroxycyclohexan-1-carboxylic acid (4b) are reported. The syntheses exploit the diastereoselective oxidation of the 5,6-double bond of the quinic acid-derived lactone 2 with osmium tetroxide.

METHOD OF OBTAINING INHIBITORS OF TYPE II DEHYDROQUINASE ENZYME AND PRECURSORS THEREOF

-

Page/Page column 15-16, (2008/06/13)

The present invention relates to a process of obtaining type II dehydroquinase enzyme inhibitors and the precursors thereof from (-)-quinic acid. The described compounds have a carboxycyclohexene structure. The process of preparing the compounds and their

Parallel Solid-Phase Synthesis and Evaluation of Inhibitors of Streptomyces coelicolor Type II Dehydroquinase

González-Bello, Concepción,Lence, Emilio,Toscano, Miguel D.,Castedo, Luis,Coggins, John R.,Abell, Chris

, p. 5735 - 5744 (2007/10/03)

A series of 1-substituted and 4-substituted benzyl analogues of the known inhibitor (1S,3R,4R)-1,3,4-trihydroxy-5-cyclohexene-1-carboxylic acid has been synthesized and tested as inhibitors of Streptomyces coelicolor type II dehydroquinase. The solid-phas

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