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123419-94-3

5-<4-Bromophenylamino(methylthio)methylene>-2,2-dimethyl-4,6-dioxo-1,3-dioxane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123419-94-3 Structure

  • Basic information

    1. Product Name: 5-<4-Bromophenylamino(methylthio)methylene>-2,2-dimethyl-4,6-dioxo-1,3-dioxane
    2. Synonyms: 5-<4-Bromophenylamino(methylthio)methylene>-2,2-dimethyl-4,6-dioxo-1,3-dioxane
    3. CAS NO:123419-94-3
    4. Molecular Formula:
    5. Molecular Weight: 372.239
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123419-94-3.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: 5-<4-Bromophenylamino(methylthio)methylene>-2,2-dimethyl-4,6-dioxo-1,3-dioxane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-<4-Bromophenylamino(methylthio)methylene>-2,2-dimethyl-4,6-dioxo-1,3-dioxane(123419-94-3)
    11. EPA Substance Registry System: 5-<4-Bromophenylamino(methylthio)methylene>-2,2-dimethyl-4,6-dioxo-1,3-dioxane(123419-94-3)

  • 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: 123419-94-3(Hazardous Substances Data)

123419-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123419-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,4,1 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 123419-94:
(8*1)+(7*2)+(6*3)+(5*4)+(4*1)+(3*9)+(2*9)+(1*4)=113
113 % 10 = 3
So 123419-94-3 is a valid CAS Registry Number.

123419-94-3Relevant articles and documents

Mechanistic studies of a "declick" reaction

Meadows, Margaret K.,Sun, Xiaolong,Kolesnichenko, Igor V.,Hinson, Caroline M.,Johnson, Kenneth A.,Anslyn, Eric V.

, p. 8817 - 8824 (2019/10/16)

A kinetic analysis of a "declick" reaction is described. Compound 1, previously reported to couple an amine and a thiol (i.e. "click") under mild aqueous conditions to create 2, undergoes release of the unaltered coupling partners upon triggering with dit

Convenient synthesis of 5-(arylamino(alkylthio)methylene)-2,2-dimethyl-1,3-dioxane-4,6-diones and 2-arylthio-4-quinolones

Tang, Jing,Huang, Xian

, p. 140 - 141 (2007/10/03)

Meldrum's acid reacted with an aryl isothiocynate and alkyl halides to afford the 5-(arylamino(alkylthio)methylene)-5-methylthio-2,2-dimethyl-1,3-dioxane-4, 6-diones and the compounds underwent thermal cyclization to give the 4-2-arylthio-4(1H)-quinolones.

Synthesis of 2-amino-1,4-dihydro-4-quinolinones and diaminomethylene Meldrum's acids derivatives as potential potassium channel openers

Erb, Benedicte,Rigo, Benoit,Pirotte, Bernard,Couturier, Daniel

, p. 15 - 28 (2007/10/03)

Starting from 5-bismethylthiomethylene Meldrum's acid, the synthesis of 5-diaminomethylene Meldrum's acids and 2-aminoquinolone derivatives, structurally related to potassium channels openers pinacidil and diazoxide, is described.

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