2-THIAZOLYLZINC BROMIDE

Product Information

Molecular Formula:
C3H2BrNSZn
Molecular Weight:
229.41
Description
2-THIAZOLYLZINC BROMIDE is a versatile biomedical agent employed for targeted therapeutic intervention against specific ailments. 2-THIAZOLYLZINC BROMIDE is a useful reagent in organic synthesis, especially in the formation of carbon-nitrogen and carbon-carbon bonds. It can be widely used in cross-coupling reactions, asymmetric allylation, synthesis of heterocyclic compounds, and the generation of amides and imides.
Synonyms
2-THIAZOLYLZINC BROMIDE; 2-THIAZOLYLZINC BROMIDE, 0.5M SOLUTION I N TETRAHYDROFURAN; 2-thiazolylzinc bromide solution
IUPAC Name
bromozinc(1+)2H-1,3-thiazol-2-ide
Canonical SMILES
C1=CS[C-]=N1.[Zn+]Br
InChI
InChI=1S/C3H2NS.BrH.Zn/c1-2-5-3-4-1/h1-2H1H/q-1+2/p-1
InChI Key
YORIBCPQDAVKHG-UHFFFAOYSA-M
Flash Point
1.4 °F - closed cup
Density
0.992 g/mL at 25 °C
Appearance
Brown Liquid
Storage
2-8°C

Safety Information

Hazards
H225 - H302 - H314 - H335 - H351
Precautionary Statement
P210 - P260 - P280 - P305 + P351 + P338 - P370 + P378 - P403 + P235

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
0
Exact Mass
226.83827 g/mol
Monoisotopic Mass
226.83827 g/mol
Topological Polar Surface Area
37.7Ų
Heavy Atom Count
7
Formal Charge
0
Complexity
83
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
2
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
WO-2020245246-A1 Alternative process for the preparation of 4-phenyl-5-alkoxycarbonyl-2-thiazol-2-yl-1,4-dihydropyrimidin-6-yl]methyl]-3-oxo-5,6,8,8a-tetrahydro-1h-imidazo[1,5-a]pyrazin-2-yl]-carboxylic acid 2019-06-06
TW-202112781-A Alternative process for the preparation of 4-phenyl-5-alkoxycarbonyl-2-thiazol-2-yl-1,4-dihydropyrimidin-6-yl]methyl]-3-oxo-5,6,8,8a-tetrahydro-1h-imidazo[1,5-a]pyrazin-2-yl]-carboxylic acid 2019-06-06
AU-2020288329-A1 Alternative process for the preparation of 4-phenyl-5-alkoxycarbonyl-2-thiazol-2-yl-1,4-dihydropyrimidin-6-yl)methyl)-3-oxo-5,6,8,8a-tetrahydro-1H-imidazo(1,5-a)pyrazin-2-yl)-carboxylic acid 2019-06-06
CA-3142659-A1 Alternative process for the preparation of 4-phenyl-5-alkoxycarbonyl-2-thiazol-2-yl-1,4-dihydropyrimidin-6-yl]methyl]-3-oxo-5,6,8,8a-tetrahydro-1h-imidazo[1,5-a]pyrazin-2-yl]-carboxylic acid 2019-06-06
CN-114026095-A Alternative process for the preparation of 4-phenyl-5-alkoxycarbonyl-2-thiazol-2-yl-1, 4-dihydropyrimidin-6-yl ] methyl ] -3-oxo-5, 6,8,8 a-tetrahydro-1H-imidazo [1,5-a ] pyrazin-2-yl ] -carboxylic acid 2019-06-06
KR-20220018486-A 4-phenyl-5-alkoxycarbonyl-2-thiazol-2-yl-1,4-dihydropyrimidin-6-yl]methyl]-3-oxo-5,6,8,8a-tetrahydro- Alternative method for preparing 1H-imidazo[1,5-a]pyrazin-2-yl]-carboxylic acid 2019-06-06
JP-WO2020004521-A1 Therapeutic agents for inflammatory, autoimmune, fibrotic, and cancerous diseases 2018-06-27
BR-112019010571-A2 compound and pharmacologically acceptable salt thereof 2016-12-26
AU-2012322572-A1 Protein kinase inhibitors 2011-10-10
AU-2012322572-B2 Protein kinase inhibitors 2011-10-10
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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