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175885-93-5

2-chloro-3-amino-1,4-naphthalenedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 175885-93-5 Structure

  • Basic information

    1. Product Name: 2-chloro-3-amino-1,4-naphthalenedione
    2. Synonyms: 2-chloro-3-amino-1,4-naphthalenedione
    3. CAS NO:175885-93-5
    4. Molecular Formula:
    5. Molecular Weight: 343.766
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 175885-93-5.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: 2-chloro-3-amino-1,4-naphthalenedione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-chloro-3-amino-1,4-naphthalenedione(175885-93-5)
    11. EPA Substance Registry System: 2-chloro-3-amino-1,4-naphthalenedione(175885-93-5)

  • 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: 175885-93-5(Hazardous Substances Data)

175885-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 175885-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,8,8 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 175885-93:
(8*1)+(7*7)+(6*5)+(5*8)+(4*8)+(3*5)+(2*9)+(1*3)=195
195 % 10 = 5
So 175885-93-5 is a valid CAS Registry Number.

175885-93-5Downstream Products

175885-93-5Relevant articles and documents

Synthesis and in Vitro Biological Evaluation of Aminonaphthoquinones and Benzo[ b ]phenazine-6,11-dione Derivatives as Potential Antibacterial and Antifungal Compounds

Tuyun, Ama? Fatih,Bayrak, Nilüfer,Yldrm, Hatice,Onul, Nihal,Mataraci Kara, Emel,Ozbek Celik, Berna

, (2015)

A series of 2-arylamino-3-chloro-1,4-naphthoquinone derivatives (3a-h) by the reaction of 2,3-dichloro-1,4-naphthoquinone with aryl amines (2a-h) and benzo[b]phenazine-6,11-dione derivatives (4a-c) by the treatment of 2-arylamino-3-chloro-1,4-naphthoquino

Crystal structure of 2-(3,5-dimethoxyphenylamino)-3-chloronaphthalene-1,4-dione

Bayrak, Nilüfer,Y?ld?z, Mahmut,Y?ld?r?m, Hatice,Sahin, Musa,Tuyun, Ama? Fatih

, p. 603 - 608 (2018)

2-(3,5-Dimethoxyphenylamino)-3-chloronaphthalene-1,4-dione compound was prepared from the nucleophilic substitution reaction of 2,3-dichloro-1,4-naphthoquinone with 3,5-dimethoxyphenylamine at reflux temperature according to literature reported previously

Synthesis, computational study, and evaluation of in vitro antimicrobial, antibiofilm, and anticancer activities of new sulfanyl aminonaphthoquinone derivatives

Bayrak, Nilufer,Yildirim, Hatice,Tuyun, Ama? Fatih,Kara, Emel Mataraci,Celik, Berna Ozbek,Gupta, Girish Kumar,Ciftci, Halil I.,Fujita, Mikako,Otsuka, Masami,Nasiri, Hamid R.

, p. 647 - 661 (2017/07/15)

Background: A set of novel sulfanyl aminonaphthoquinone derivatives (5a-j) were synthesized starting from 2,3-dichloro-1,4-naphthoquinone (1). The amine substituents were introduced via a nucleophilic substitution at reflux temperature. Subsequent reactio

Synthesis and characterization of nitrogen and sulfur containing 1,4-naphthoquinones

Sayil, Cigdem,Kurban, Semih,Ibis, Cemil

, p. 1855 - 1867 (2013/11/06)

New N,S-disubstituted naphthoquinones were synthesized by reactions of S- and N-nucleophiles with 2,3-dichloro-1,4-naphthoquinone. 2-(Hexadecylthio)-3- (phenylamino)-naphthalene-1,4-dione 5a was synthesized by reaction of 2-chloro-3-(phenylamino)-naphthal

Design of antineoplastic agents on the basis of the '2-phenylnaphthalene-type' structural pattern. 3. Synthesis and biological activity evaluation of 5H-benzo[b]naphtho[2,3 d]pyrrole-6,11-dione derivatives

Luo,Chou,Cheng

, p. 113 - 117 (2007/10/03)

A number of 5H-Benzo[b]naphtho[2,3-d]pyrrole-6,11-dione derivatives were synthesized. Their biological activity was compared with that of the corresponding benzoxazolo- and benzthiazolo-analogues.

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