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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)-

Benzamide, 2-(acetyloxy)-N-(5-nitro-2-thiazolyl)-

CC(=O)Oc1ccccc1C(=O)Nc1ncc(s1)[N+](=O)[O-] Request for Quotation
Chemical Name: Benzamide, 2-(acetyloxy)-N-(5-nitro-2-thiazolyl)-
CAS Number: 55981-09-4
Product Number: AG00I9ZK(AGN-PC-0JKS8J)
Synonyms:
MDL No:
Molecular Formula: C12H9N3O5S
Molecular Weight: 307.2820

Identification/Properties

Computed Properties
Molecular Weight:
307.28g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
4
Exact Mass:
307.026g/mol
Monoisotopic Mass:
307.026g/mol
Topological Polar Surface Area:
142A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
428
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Acetyloxy)-N-(5-nitro-2-thiazolyl)benzamide, commonly used in chemical synthesis, serves as a versatile building block in the creation of novel organic compounds. With its unique structure and reactivity, this compound plays a crucial role in the formation of pharmaceuticals, agrochemicals, and materials science applications. By acting as a key intermediate, it facilitates the synthesis of complex molecules with enhanced biological activities or tailored properties. Through strategic manipulations of its functional groups, chemists can harness its potential to construct a diverse range of target molecules, thus driving innovation and advancement in chemical research and development.