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CAS

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1456706-37-8

3-chloro-2-(4-methoxyanilino)-5,5-dimethyl-5,6,7,8-tetrahydroanthracene-1,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1456706-37-8 Structure

  • Basic information

    1. Product Name: 3-chloro-2-(4-methoxyanilino)-5,5-dimethyl-5,6,7,8-tetrahydroanthracene-1,4-dione
    2. Synonyms: 3-chloro-2-(4-methoxyanilino)-5,5-dimethyl-5,6,7,8-tetrahydroanthracene-1,4-dione
    3. CAS NO:1456706-37-8
    4. Molecular Formula:
    5. Molecular Weight: 395.886
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1456706-37-8.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: 3-chloro-2-(4-methoxyanilino)-5,5-dimethyl-5,6,7,8-tetrahydroanthracene-1,4-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-chloro-2-(4-methoxyanilino)-5,5-dimethyl-5,6,7,8-tetrahydroanthracene-1,4-dione(1456706-37-8)
    11. EPA Substance Registry System: 3-chloro-2-(4-methoxyanilino)-5,5-dimethyl-5,6,7,8-tetrahydroanthracene-1,4-dione(1456706-37-8)

  • 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: 1456706-37-8(Hazardous Substances Data)

1456706-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1456706-37-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,6,7,0 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1456706-37:
(9*1)+(8*4)+(7*5)+(6*6)+(5*7)+(4*0)+(3*6)+(2*3)+(1*7)=178
178 % 10 = 8
So 1456706-37-8 is a valid CAS Registry Number.

1456706-37-8Downstream Products

1456706-37-8Relevant articles and documents

New 1,4-anthracenedione derivatives with fused heterocyclic rings: Synthesis and biological evaluation

Castro, Ma. ngeles,Gamito, Ana Ma.,Tangarife-Castao, Vernica,Roa-Linares, Vicky,Miguel Del Corral, Jos Ma.,Mesa-Arango, Ana C.,Betancur-Galvis, Liliana,Francesch, Andrs M.,San Feliciano, Arturo

, p. 1244 - 1261 (2015)

Several terpenylquinones derived from 1,4-anthracenedione (1,4-anthracenequinone, AQ) have been prepared by addition or substitution nucleophilic reactions and further transformed into extended polycyclic systems, which mainly kept the 1,4-quinone moiety fused to different nitrogen-heterocyclic rings (pyrrole, imidazole, pyrazine or quinoxaline) into the structure. The compounds synthesized were evaluated for their antineoplastic, antifungal and antiviral activities. GI50 antineoplastic values remained under μM levels for AQs, while the heterocyclic derivatives showed antifungal MIC values in the low μg mL-1 range against yeasts and filamentous fungi. Only few compounds displayed a discrete non-selective antiherpetic activity in the μg mL-1 range. This journal is

Synthesis and antifungal activity of terpenyl-1,4-naphthoquinone and 1,4-anthracenedione derivatives

Castro, Ma Angeles,Gamito, Ana Ma,Tangarife-Castano, Veronica,Zapata, Bibiana,Miguel Del Corral, Jose Ma,Mesa-Arango, Ana C.,Betancur-Galvis, Liliana,San Feliciano, Arturo

, p. 19 - 27 (2013/10/01)

The antifungal evaluation of twenty seven simple and heterocycle-fused prenyl-1,4-naphthoquinones and 1,4-anthracenediones was performed in vitro against human pathogenic yeasts (Candida spp.) and filamentous fungi (Aspergillus spp., Fusarium spp., and Tr

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