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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-amino-1,3-thiazole-5-carbaldehyde;hydrochloride

Nc1ncc(s1)C=O.Cl Request for Quotation
Chemical Name: 2-amino-1,3-thiazole-5-carbaldehyde;hydrochloride
CAS Number: 920313-27-5
Product Number: AG006EPE(AGN-PC-07XTFP)
Synonyms:
MDL No:
Molecular Formula: C4H5ClN2OS
Molecular Weight: 164.6133

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
164.607g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
163.981g/mol
Monoisotopic Mass:
163.981g/mol
Topological Polar Surface Area:
84.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
98
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

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Aminothiazole-5-carbaldehyde hydrochloride is a versatile compound commonly used in chemical synthesis. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. With its unique structure and reactivity, this compound plays a crucial role in the development of new molecules and materials.In organic synthesis, 2-Aminothiazole-5-carbaldehyde hydrochloride can be utilized as a starting material for the preparation of heterocyclic compounds through cyclization reactions. Its presence can facilitate the introduction of the aminothiazole moiety into complex molecular structures, allowing for the modification of chemical properties and biological activities.Furthermore, this compound can be employed in the synthesis of bioactive molecules such as antiviral agents, antibacterial drugs, and enzyme inhibitors. Its versatile nature makes it a valuable tool for medicinal chemists and researchers working in the field of drug discovery.Overall, the application of 2-Aminothiazole-5-carbaldehyde hydrochloride in chemical synthesis offers a wide range of possibilities for the development of novel compounds with potential therapeutic benefits.