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209260-76-4

2-DIMETHYLAMINO-4-BROMOTHIAZOLE is a brominated thiazole derivative with the molecular formula C6H7BrN2S, commonly used in the pharmaceutical industry due to its significant antimicrobial, antifungal, and cytotoxic properties.
Used in Pharmaceutical Industry:
2-DIMETHYLAMINO-4-BROMOTHIAZOLE is used as an antimicrobial and antifungal agent for its significant properties in combating various microorganisms.
Used in Cancer Treatment Research:
2-DIMETHYLAMINO-4-BROMOTHIAZOLE is used as a cytotoxic agent in the study of cancer treatment, as it has shown to have effects on cancer cells in vitro.

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  • 209260-76-4 Structure

  • Basic information

    1. Product Name: 2-DIMETHYLAMINO-4-BROMOTHIAZOLE
    2. Synonyms: 2-DIMETHYLAMINO-4-BROMOTHIAZOLE;4-broMo-N,N-diMethylthiazol-2-aMine;2-thiazolamine,4-bromo-N,N-dimethyl-;4-Bromo-N,N-dimethyl-1,3-thiazol-2-amine
    3. CAS NO:209260-76-4
    4. Molecular Formula: C5H7BrN2S
    5. Molecular Weight: 207.09
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 209260-76-4.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-DIMETHYLAMINO-4-BROMOTHIAZOLE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-DIMETHYLAMINO-4-BROMOTHIAZOLE(209260-76-4)
    11. EPA Substance Registry System: 2-DIMETHYLAMINO-4-BROMOTHIAZOLE(209260-76-4)

  • 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: 209260-76-4(Hazardous Substances Data)

209260-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209260-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,2,6 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 209260-76:
(8*2)+(7*0)+(6*9)+(5*2)+(4*6)+(3*0)+(2*7)+(1*6)=124
124 % 10 = 4
So 209260-76-4 is a valid CAS Registry Number.

209260-76-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-N,N-dimethyl-1,3-thiazol-2-amine

1.2 Other means of identification

Product number -
Other names 4-BROMO-N,N-DIMETHYLTHIAZOL-2-AMINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:209260-76-4 SDS

209260-76-4Downstream Products

209260-76-4Relevant articles and documents

Condensed tricyclic compound and applications thereof in medicines

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Paragraph 0426-0431, (2020/04/17)

The invention relates to a condensed tricyclic compound and applications thereof in medicines, particularly to applications of the condensed tricyclic compound as a drug for treating and/or preventinghepatitis B, specifically to a compound represented by a general formula (I) or a stereoisomer, a tautomer, a nitrogen oxide, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrugthereof, wherein variables are defined in the specification. The invention further relates to applications of the compound represented by the general formula (I) or the stereoisomer, the tautomer, thenitric oxide, the solvate, the metabolite, the pharmaceutically acceptable salt or the prodrug thereof as a drug, particularly applications of the compound as a drug for treating and/or preventing hepatitis B.

Epothilone analogs

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, (2008/06/13)

Epothilone A, epothilone B, analogs of epothilone and libraries of epothilone analogs are synthesized. Epothilone A and B are known anticancer agents that derive their anticancer activity by the prevention of mitosis through the induction and stabilization of microtubulin assembly. The analogs of epothilone are novel. Several of the anlogs are demonstrated to have a superior cytotoxic activities as compared to epothilone A or epothilone B as demonstrated by their enhanced ability to induce the polymerization and stabilization of microtubules.

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