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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)-

Thiazole, 2,4-dichloro-5-nitro-

Clc1nc(c(s1)[N+](=O)[O-])Cl Request for Quotation
Chemical Name: Thiazole, 2,4-dichloro-5-nitro-
CAS Number: 107190-42-1
Product Number: AG009TDN(AGN-PC-00O8EG)
Synonyms:
MDL No:
Molecular Formula: C3Cl2N2O2S
Molecular Weight: 199.0153

Identification/Properties

Computed Properties
Molecular Weight:
199.005g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
197.906g/mol
Monoisotopic Mass:
197.906g/mol
Topological Polar Surface Area:
87A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
152
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4-Dichloro-5-nitrothiazole is a versatile chemical compound that finds application in various chemical synthesis processes. This compound is utilized primarily in the pharmaceutical and agrochemical industries for the synthesis of a wide range of important molecules. In organic synthesis, 2,4-Dichloro-5-nitrothiazole serves as a key building block in the creation of complex pharmaceutical compounds due to its unique chemical reactivity and ability to introduce specific functionalities into target molecules. By incorporating 2,4-Dichloro-5-nitrothiazole into synthesis pathways, chemists can introduce both chloro and nitro functional groups simultaneously, enabling the development of novel compounds with enhanced properties and biological activities. Furthermore, the presence of the thiazole ring in 2,4-Dichloro-5-nitrothiazole adds structural diversity and stability to the synthesized products, making it a valuable tool in the creation of structurally diverse drug candidates and agrochemicals.