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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)-

Thiophene, 4-bromo-2-nitro-

[O-][N+](=O)c1cc(cs1)Br Request for Quotation
Chemical Name: Thiophene, 4-bromo-2-nitro-
CAS Number: 85598-49-8
Product Number: AG004QHL(AGN-PC-057IH3)
Synonyms:
MDL No:
Molecular Formula: C4H2BrNO2S
Molecular Weight: 208.0332

Identification/Properties

Properties
BP:
257.6°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
208.029g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
206.899g/mol
Monoisotopic Mass:
206.899g/mol
Topological Polar Surface Area:
74.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
126
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-2-nitrothiophene is a versatile chemical compound commonly used in various chemical synthesis applications. One of its key roles is as a building block in the creation of complex organic molecules, particularly in the pharmaceutical and agrochemical industries. Due to its unique structural properties, 4-Bromo-2-nitrothiophene serves as a valuable intermediate in the synthesis of a wide range of compounds, including potential drug candidates and biologically active molecules. Its ability to undergo various chemical transformations makes it an essential reagent for the preparation of diverse chemical structures with specific functionalities. In addition, 4-Bromo-2-nitrothiophene plays a crucial role in the development of new materials and organic reactions, contributing significantly to advancements in synthetic organic chemistry.