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185351-24-0

2-CHLORO-3-([2-(1H-INDOL-3-YL)ETHYL]AMINO)NAPHTHOQUINONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 185351-24-0 Structure

  • Basic information

    1. Product Name: 2-CHLORO-3-([2-(1H-INDOL-3-YL)ETHYL]AMINO)NAPHTHOQUINONE
    2. Synonyms: 2-CHLORO-3-([2-(1H-INDOL-3-YL)ETHYL]AMINO)NAPHTHOQUINONE
    3. CAS NO:185351-24-0
    4. Molecular Formula: C20H15ClN2O2
    5. Molecular Weight: 350.8
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 185351-24-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-CHLORO-3-([2-(1H-INDOL-3-YL)ETHYL]AMINO)NAPHTHOQUINONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-CHLORO-3-([2-(1H-INDOL-3-YL)ETHYL]AMINO)NAPHTHOQUINONE(185351-24-0)
    11. EPA Substance Registry System: 2-CHLORO-3-([2-(1H-INDOL-3-YL)ETHYL]AMINO)NAPHTHOQUINONE(185351-24-0)

  • 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: 185351-24-0(Hazardous Substances Data)

185351-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185351-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,3,5 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 185351-24:
(8*1)+(7*8)+(6*5)+(5*3)+(4*5)+(3*1)+(2*2)+(1*4)=140
140 % 10 = 0
So 185351-24-0 is a valid CAS Registry Number.

185351-24-0Downstream Products

185351-24-0Relevant articles and documents

On the synthesis of naphthoquinonyl heterocyclic amino acids

Shrestha-Dawadi, Prativa Bade,Bittner, Shmuel,Fridkin, Mati,Rahimipour, Shai

, p. 1468 - 1472 (2007/10/03)

L-Histidine, N(α)-cbz-L-histidine, L-tryptophan and L-proline react with 1,4-naphthoquinone or 2,3-dichloro-1,4-naphthoquinone to afford modified N-quinonyl amino acids. With free α-amino acids, the quinone moiety is attached to the α-amino group. With blocked α-amino acids the quinone moiety is attached to the heterocyclic nitrogen atom.

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