CAS No.502145-18-8 | 4-Bromo-2-thiazolamine
CAS No.502145-18-8 | 4-Bromo-2-thiazolamine
CAS No.502145-18-8 | 4-Bromo-2-thiazolamine
CAS No.502145-18-8 | 4-Bromo-2-thiazolamine
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  • CAS No.502145-18-8 | 4-Bromo-2-thiazolamine
  • CAS No.502145-18-8 | 4-Bromo-2-thiazolamine
  • CAS No.502145-18-8 | 4-Bromo-2-thiazolamine
  • CAS No.502145-18-8 | 4-Bromo-2-thiazolamine

CAS No.502145-18-8 | 4-Bromo-2-thiazolamine

Name: 4-Bromo-2-thiazolamine CAS No.502145-18-8 MF: C3H3BrN2S MW: 179.04 Purity:97% Package: 5g,25g,100g,500g,1kg,25kg Worldwide Delivery

Categories:

Analytical Chemicals

Product introduction

Introduction and application of CAS No.502145-18-8 | 4-Bromo-2-thiazolamine

2-Amino-4-bromothiazole is used to prepare coumarin derivatives with antibacterial properties.

4-Bromo-2-thiazolamine is an anticarcinogenic agent that belongs to the class of methoxy, acetylation, synthetic methods. It has been shown to induce DNA fragmentation and inhibit cell proliferation in vitro. 4-Bromo-2-thiazolamine inhibits cancer in mice with melanoma and human liver cancer cells by inducing apoptosis. The anticancer activity of this compound may be due to its ability to inhibit the growth of cancer cells by interfering with protein synthesis.

Synonyms:

4-BROMO-THIAZOL-2-YLAMINE;
2-Amino-4-bromothiazole;
2-ThiazolaMine,4-broMo-;
4-BroMo-thiazole-2-ylaMine;
4-broMothiazol-2-aMinehydrochloride;
4-broMo-1,3-thiazol-2-aMine;
4-Bromo-1,3-thiazol-2-amine98%

 

Specification of CAS No.502145-18-8 | 4-Bromo-2-thiazolamine

CAS No.

502145-18-8

MF

C3H3BrN2S

MW

179.04

Boiling point

287.6±13.0 °C(Predicted)

Density(25℃,g/cm3)

1.976±0.06 g/cm3(Predicted)

acidity coefficient(pKa)

2.17±0.10(Predicted)

Package of CAS No.502145-18-8 | 4-Bromo-2-thiazolamine

Package:100g; 500g; 1kg; 25kg;bulk package

Transportation: by courier/ by air/ by sea

Related Articles of CAS No.502145-18-8 | 4-Bromo-2-thiazolamine

 

Thiazoles and Benzothiazoles

YJ Wu - Metalation of Azoles and Related Five-Membered Ring …, 2012 - Springer

… Easy access to a series of 5-substituted 4-bromo-2-thiazolamine derivatives 49 is based on
the halogen dance reaction [29]. Addition of 3.3 eq. LDA to 4-bromothiazole 46 at 0C results …

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