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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)-

Carbonic acid, 4-nitrophenyl 5-thiazolylmethyl ester

O=C(Oc1ccc(cc1)[N+](=O)[O-])OCc1cncs1 Request for Quotation
Chemical Name: Carbonic acid, 4-nitrophenyl 5-thiazolylmethyl ester
CAS Number: 144163-97-3
Product Number: AG001J1B(AGN-PC-07Y4WV)
Synonyms:
MDL No:
Molecular Formula: C11H8N2O5S
Molecular Weight: 280.2566

Identification/Properties

Properties
MP:
65-67°C
BP:
475.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
280.254g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
5
Exact Mass:
280.015g/mol
Monoisotopic Mass:
280.015g/mol
Topological Polar Surface Area:
123A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
328
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The chemical compound ((5-Thiazolyl)methyl)-(4-nitrophenyl)carbonate, also known as $name$, plays a crucial role in chemical synthesis due to its unique properties. This compound serves as a versatile building block in organic chemistry, particularly in the development of pharmaceuticals and agrochemicals. Its distinct structure allows for incorporation into a wide range of molecular frameworks, enabling the synthesis of diverse compounds with enhanced biological activities. Furthermore, the reactivity of $name$ facilitates the creation of structurally complex molecules with improved efficiency, making it a valuable tool in the field of medicinal chemistry. By leveraging the synthetic capabilities of ((5-Thiazolyl)methyl)-(4-nitrophenyl)carbonate, researchers can expedite the discovery and development of novel compounds with potential applications in various industries.