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CAS

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24326-89-4

2-Azabicyclo[2.2.1]heptan-3-one, 1,7,7-trimethyl-, (1R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 24326-89-4 Structure

  • Basic information

    1. Product Name: 2-Azabicyclo[2.2.1]heptan-3-one, 1,7,7-trimethyl-, (1R)-
    2. Synonyms:
    3. CAS NO:24326-89-4
    4. Molecular Formula: C9H15NO
    5. Molecular Weight: 153.224
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24326-89-4.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: 2-Azabicyclo[2.2.1]heptan-3-one, 1,7,7-trimethyl-, (1R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Azabicyclo[2.2.1]heptan-3-one, 1,7,7-trimethyl-, (1R)-(24326-89-4)
    11. EPA Substance Registry System: 2-Azabicyclo[2.2.1]heptan-3-one, 1,7,7-trimethyl-, (1R)-(24326-89-4)

  • 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: 24326-89-4(Hazardous Substances Data)

24326-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24326-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,2 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24326-89:
(7*2)+(6*4)+(5*3)+(4*2)+(3*6)+(2*8)+(1*9)=104
104 % 10 = 4
So 24326-89-4 is a valid CAS Registry Number.

24326-89-4Relevant articles and documents

Toward the development of a general chiral auxiliary. 9. Highly diastereoselective alkylations and acylations to form tertiary and quaternary centers.

Boeckman Jr.,Boehmler,Musselman

, p. 3777 - 3780 (2007/10/03)

[reaction--see text] Enolates of a new camphor-derived lactam auxiliary are shown to monoalkylate with very high diastereoselectivity. A second alkylation occurs with reactive alkylating agents to afford quaternary centers also with high diastereoselectiv

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