- Thiazole,
or 1,3-thiazole,
is a heterocyclic
compound that contains
both sulfur and nitrogen; the term 'thiazole' also refers to a large
family of derivatives.
- Thiazole
itself is a pale yellow liquid with a
pyridine-like odor and the molecular formula C3H3NS.
- The
thiazole ring is notable as a component of the vitamin
thiamine (B1).
- Thiazoles are found is a variety of
specialized products, often fused with benzene derivatives, the
so-called benzothiazoles.
- In addition to vitamin
B1, the thiazole ring is found
in epothilone. Other important thiazole derivatives
are benzothiazoles, for example, the firefly
chemical luciferin.
- Thiazoles are members of
the azoles heterocycles that
includes imidazoles and oxazoles.
- Thiazole can also be
considered a functional group. Oxazoles are related compounds,
with sulfur replaced by oxygen.
- Thiazoles are
structurally similar to imidazoles, with the thiazole
sulfur replaced by nitrogen.
- Thiazole is
used for manufacturing biocides, fungicides, pharmaceuticals, and
dyes.
- It is
soluble in alcohol and ether and slightly soluble in
water.
- It is
parent material for numerous of chemical compounds including sulfur
drugs, biocides, fungicides, dyes, chemical reaction
accelerators.
- With Halon
reaction, alkylation and three nitrogen to form thiazole Smith Weng 3
(thiazonium) salt.
- Chlorine
acetaldehyde and Thiobarbituric formamide response from the system. Some
drugs (such as penicillin, sulfa drug), Dye (such as acrylic fiber with
a cationic INNOVATIVE red), rubber accelerator, color purity and so the
film has thiazole ring.
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General
- Thiazole
- General Information
- Identification,
Properties
- General facts
- Thiazole facts
Synthesis
- Design, Synthesis and in
vitro Evaluation of Thiazole Derivatives of Ibuprofen as
Cyclooxygenase-2 Inhibitors
- Synthesis and investigation of new Functionalized
2-aminothiazole and 2-aminoselenazole derivatives
- Multicomponent One-Pot
Synthesis of Substituted Hantzsch Thiazole Derivatives Under Solvent
Free Conditions
- Preparation of Thiazole
- Biosynthesis of the thiazole moiety of thiamin in
Escherichia coli
Properties &
Products
- Basic and solid
properties
- Physical and Chemical
Properties
- Properties of
Thiazole
- Thiazole - Properties
- List of products containing
Thiazole
Company profiles &
Suppliers
- Company from China
- Company from U.S.A
- Company from Michigan,
U.S.A
- Thiazole suppliers
- Suppliers of Thiazole
- Thiazole exporters
Data sheets
- Thiazole Orange
- Thiabzole 500 SC
- 2-Chloro-1,3-thiazole
- 4-(beta-aminoethyl)thiazole
- 1,3-Thiazole-2-carbonyl
chloride
- 2-amino-5-methyl-4-phenyl-Thiazole
- Thiazole, 99%
- 6-Methylimidazo[2,1-b][1,3]thiazole-5-carbohydrazide,
97%
-
Thiazole, 99%
MSDS
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Patent
- Thiazole derivatives
- Thiazoles
- Morpholino pyridyl thiazole
compound
- Substituted thiazoles
- 2-(3,4,5-Trimethoxyphenyl)-4,5-disubstituted
thiazoles
- Substituted thiazoles as
immunoregulants
- 2,5-Dipicryl
thiazoles
- Aryl-substituted
thiazoles
- 5-lipoxygenase inhibiting
thiazoles
- Thiazole derivatives and use
thereof
- Thiazole cardiovascular
agents
- Guanidino imidazoles and
thiazoles
- Substituted diazoles and
thiazoles
Reports
- Thiazoles: A Valuable
Insight into the Recent Advances and Biological Activities
- A new and efficient
preparation of 2-aminothiazole-5-carbamides:
applications to the
synthesis of the anti-cancer drug dasatinib
- The Preparation C-4 Thiazole
and Wittig Condensations of Phosphonium Methylides
- Thiazole Research
- A versatile multicomponent
one-pot synthesis of Thiazole derivatives under solvent free conditions:
Designed by pass showed antiviral activity as predicted
- Structure of the Thiazole
Biosynthetic Enzyme THI1 from
Arabidopsis thaliana
- Metabolism of Physiological
Doses of Thiazole-2-14Clabeled
Thiamine by the Rat
- Thiazole: A valuable insight
into recent advances, synthesis and
biological activities
- Biological Activity
of 4-Substituted Methoxybenzoyl- Aryl-Thiazole: An Active Microtubule
Inhibitor
- Thiazole,
Oxadiazole, and Carboxamide Derivatives of Artemisinin are Highly
Selective and Potent Inhibitors of Toxoplasma
gondii
- Endeavour launches
thiazoles for cancer research
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