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35468-15-6

(cyclohexyl)chloroacetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 35468-15-6 Structure

  • Basic information

    1. Product Name: (cyclohexyl)chloroacetic acid
    2. Synonyms: (cyclohexyl)chloroacetic acid
    3. CAS NO:35468-15-6
    4. Molecular Formula:
    5. Molecular Weight: 176.643
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 35468-15-6.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: (cyclohexyl)chloroacetic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (cyclohexyl)chloroacetic acid(35468-15-6)
    11. EPA Substance Registry System: (cyclohexyl)chloroacetic acid(35468-15-6)

  • 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: 35468-15-6(Hazardous Substances Data)

35468-15-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35468-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,6 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 35468-15:
(7*3)+(6*5)+(5*4)+(4*6)+(3*8)+(2*1)+(1*5)=126
126 % 10 = 6
So 35468-15-6 is a valid CAS Registry Number.

35468-15-6Relevant articles and documents

Enantioselective organocatalytic synthesis of 2-oxopiperazines from aldehydes: Identification of the elusive epoxy lactone intermediate

Kaplaneris, Nikolaos,Spyropoulos, Constantinos,Kokotou, Maroula G.,Kokotos, Christoforos G.

, p. 5800 - 5803 (2016)

An organocatalytic linchpin catalysis approach was envisaged to convert simple aldehydes into enantioenriched 2-oxopiperazines. A four-step reaction sequence (chlorination, oxidation, substitution, and cyclization) was developed and led to different substitution patterns in high yields and selectivities. The reaction mechanism was studied, and the previously elusive epoxy lactone intermediate was identified by HRMS.

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