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CAS

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145874-04-0

Bicyclo[2.2.1]hept-2-en-2-yl-[(1S,2R,3S,4R)-3-(3-hydroxy-phenyl)-bicyclo[2.2.1]hept-2-yl]-methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 145874-04-0 Structure

  • Basic information

    1. Product Name: Bicyclo[2.2.1]hept-2-en-2-yl-[(1S,2R,3S,4R)-3-(3-hydroxy-phenyl)-bicyclo[2.2.1]hept-2-yl]-methanone
    2. Synonyms:
    3. CAS NO:145874-04-0
    4. Molecular Formula:
    5. Molecular Weight: 308.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 145874-04-0.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: Bicyclo[2.2.1]hept-2-en-2-yl-[(1S,2R,3S,4R)-3-(3-hydroxy-phenyl)-bicyclo[2.2.1]hept-2-yl]-methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: Bicyclo[2.2.1]hept-2-en-2-yl-[(1S,2R,3S,4R)-3-(3-hydroxy-phenyl)-bicyclo[2.2.1]hept-2-yl]-methanone(145874-04-0)
    11. EPA Substance Registry System: Bicyclo[2.2.1]hept-2-en-2-yl-[(1S,2R,3S,4R)-3-(3-hydroxy-phenyl)-bicyclo[2.2.1]hept-2-yl]-methanone(145874-04-0)

  • 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: 145874-04-0(Hazardous Substances Data)

145874-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145874-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,8,7 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 145874-04:
(8*1)+(7*4)+(6*5)+(5*8)+(4*7)+(3*4)+(2*0)+(1*4)=150
150 % 10 = 0
So 145874-04-0 is a valid CAS Registry Number.

145874-04-0Downstream Products

145874-04-0Relevant articles and documents

Palladium-catalyzed norbornene-carbon monoxide co-oligomerization initiated by aryl groups and terminated by double bond formation

Dalcanale, E.,An, Z.,Battaglia, L. P.,Catellani, M.,Chiusoli, G. P.

, p. 375 - 388 (1992)

The use of m-iodophenol as initiator in palladium-catalyzed norbornene-carbon monoxide oligomerization in the presence of potassium acetate unexpectedly leads to termination by double bond formation in spite of the limitations to β-H-anti elimination.The presence of endo products points to preliminary exo-to-endo isomerization through enolization.The X-ray structure of one stereoisomer (Ia) is given.

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