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CAS

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350252-92-5

4-acetyl-4-benzylpimelic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 350252-92-5 Structure

  • Basic information

    1. Product Name: 4-acetyl-4-benzylpimelic acid
    2. Synonyms: 4-acetyl-4-benzylpimelic acid
    3. CAS NO:350252-92-5
    4. Molecular Formula:
    5. Molecular Weight: 292.332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 350252-92-5.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: 4-acetyl-4-benzylpimelic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-acetyl-4-benzylpimelic acid(350252-92-5)
    11. EPA Substance Registry System: 4-acetyl-4-benzylpimelic acid(350252-92-5)

  • 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: 350252-92-5(Hazardous Substances Data)

350252-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 350252-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,0,2,5 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 350252-92:
(8*3)+(7*5)+(6*0)+(5*2)+(4*5)+(3*2)+(2*9)+(1*2)=115
115 % 10 = 5
So 350252-92-5 is a valid CAS Registry Number.

350252-92-5Relevant articles and documents

Synthesis of substituted tricyclo[5.3.1.04,9]undecan-2,6-diones

Giasuddin Ahmed,Iqbal Moeiz, Syed M,Asghari Ahmed,Kiuchi, Fumiyuki,Tsuda, Yoshisuke

, p. 3143 - 3150 (2007/10/03)

The morpholine enamines of 4-acetyl-4-phenylcyclohexanone 3a, 4-acetyl-4-isopropenylcyclohexanone 3b, 4-acetyl-4-methylcyclohexanone 3c react with acryloyl chloride to give 1-phenyl-4(N-morpholino)tricyclo[5.3.1.04,9]undecan-2,6-dione 9a, 1-isopropenyl-4(N-morpholino)tricyclo[5.3.1.04,9]undecan-2,6-dione 9b, and 1-methyl-4(N-morpholino)tricyclo[5.3.1.04,9]undecan-2,6-dione 9c, respectively, along with the corresponding substituted adamantane-2,4-diones. The morpholine enamine of 4-acetyl-4-benzylcyclohexa-none 3d and pyrrolidine enamine of 4-acetyl-4-phenylcyclohexanone 3a yield the corresponding 1-benzyl-4(N-morpholino)tricyclo[5.3.1.04,9]undecan-2,6-dione 9d and 8(R)-methyl-1-phenyl-4(N-pyrrolidinyl)tricyclo[5.3.1.04,9] undecan-2,6-dione 9e. No substituted adamantane-2,4-diones were formed in any of the latter two reactions.

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