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CAS

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1619232-16-4

dodecan-1-aminium 4-chloro-2-[(2-chloro-4-nitrophenyl)carbamoyl]phenoxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1619232-16-4 Structure

  • Basic information

    1. Product Name: dodecan-1-aminium 4-chloro-2-[(2-chloro-4-nitrophenyl)carbamoyl]phenoxide
    2. Synonyms:
    3. CAS NO:1619232-16-4
    4. Molecular Formula:
    5. Molecular Weight: 512.477
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1619232-16-4.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: dodecan-1-aminium 4-chloro-2-[(2-chloro-4-nitrophenyl)carbamoyl]phenoxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: dodecan-1-aminium 4-chloro-2-[(2-chloro-4-nitrophenyl)carbamoyl]phenoxide(1619232-16-4)
    11. EPA Substance Registry System: dodecan-1-aminium 4-chloro-2-[(2-chloro-4-nitrophenyl)carbamoyl]phenoxide(1619232-16-4)

  • 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: 1619232-16-4(Hazardous Substances Data)

1619232-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1619232-16-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,9,2,3 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1619232-16:
(9*1)+(8*6)+(7*1)+(6*9)+(5*2)+(4*3)+(3*2)+(2*1)+(1*6)=154
154 % 10 = 4
So 1619232-16-4 is a valid CAS Registry Number.

1619232-16-4Downstream Products

1619232-16-4Relevant articles and documents

Modification of the anticestodal drug 5-chloro-N-(2-chloro-4-nitrophenyl)- 2-hydroxybenzamide with a view to improve its biological effect

Galkina,Chubukaeva,Bakhtiyarova,Galkin,Cherkasov,Islamov,Kataeva

, p. 800 - 804 (2014)

Reactions of 5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide, the active substance of the drug Niclosamide (Phenasal), with higher amines (dodecan-1-amine, hexadecan-1-amine) and 1-(2-aminoethyl)-piperazine lead to the formation of the corresponding water-soluble ammonium salts with retention of pharmacophoric groups responsible for the antihelminthic effect, whereas no nucleophilic aromatic substitution of chlorine is observed. The product structure was determined by X-ray analysis.

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