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CAS

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72204-08-1

Bicyclo[2.2.1]hept-5-ene-2-carboxaldehyde, 2-methyl-, (1R,2S,4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 72204-08-1 Structure

  • Basic information

    1. Product Name: Bicyclo[2.2.1]hept-5-ene-2-carboxaldehyde, 2-methyl-, (1R,2S,4R)-
    2. Synonyms:
    3. CAS NO:72204-08-1
    4. Molecular Formula: C9H12O
    5. Molecular Weight: 136.194
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 72204-08-1.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-5-ene-2-carboxaldehyde, 2-methyl-, (1R,2S,4R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Bicyclo[2.2.1]hept-5-ene-2-carboxaldehyde, 2-methyl-, (1R,2S,4R)-(72204-08-1)
    11. EPA Substance Registry System: Bicyclo[2.2.1]hept-5-ene-2-carboxaldehyde, 2-methyl-, (1R,2S,4R)-(72204-08-1)

  • 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: 72204-08-1(Hazardous Substances Data)

72204-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72204-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,2,0 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72204-08:
(7*7)+(6*2)+(5*2)+(4*0)+(3*4)+(2*0)+(1*8)=91
91 % 10 = 1
So 72204-08-1 is a valid CAS Registry Number.

72204-08-1Relevant articles and documents

Enantioselective diels-alder reactions with anomalous endo/exo selectivities using conformationally flexible chiral supramolecular catalysts

Hatano, Manabu,Mizuno, Tomokazu,Izumiseki, Atsuto,Usami, Ryota,Asai, Takafumi,Akakura, Matsujiro,Ishihara, Kazuaki

scheme or table, p. 12189 - 12192 (2012/02/01)

Swapped selectivities: The use of tailor-made catalysts results in anomalous endo/exo selectivities and high enantioselectivities in the Diels-Alder reactions of cyclopentadiene with different acroleins (see scheme). These supramolecular catalysts are prepared in situ from chiral diols, arylboronic acid, and tris(pentafluorophenyl)borane, and can discriminate the re/si face of the dienophile as well as the endo/exo approach of the diene.

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