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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-Thiophenecarboxamide, 5-bromo-

NC(=O)c1ccc(s1)Br Request for Quotation
Chemical Name: 2-Thiophenecarboxamide, 5-bromo-
CAS Number: 76371-66-9
Product Number: AG003ML6(AGN-PC-0JTO64)
Synonyms:
MDL No:
Molecular Formula: C5H4BrNOS
Molecular Weight: 206.0604

Identification/Properties

Properties
MP:
77-78 °C
BP:
318 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
206.057g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
204.92g/mol
Monoisotopic Mass:
204.92g/mol
Topological Polar Surface Area:
71.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
130
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-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromothiophene-2-carboxamide is a versatile compound widely used in chemical synthesis as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure and reactivity, this compound is particularly valued for its ability to participate in a range of important synthetic reactions, making it an essential tool for researchers and chemists in the development of new compounds.As a key intermediate in the synthesis of complex organic molecules, 5-Bromothiophene-2-carboxamide serves as a valuable starting material for the introduction of functional groups and the formation of bonds in organic chemistry. Its presence in the molecular structure of target compounds often imparts specific properties and functionalities desired for various applications.In pharmaceutical synthesis, 5-Bromothiophene-2-carboxamide plays a crucial role in the development of new drug candidates, allowing chemists to modify and optimize molecular structures to enhance biological activity, improve pharmacokinetic properties, and reduce undesirable side effects. By incorporating this compound into drug design, researchers can explore new therapeutic avenues and address unmet medical needs.Furthermore, in agrochemical research, 5-Bromothiophene-2-carboxamide finds applications in the creation of crop protection products, herbicides, and insecticides. Its unique chemical properties enable scientists to design effective and environmentally friendly agricultural solutions that help increase crop yields, improve plant health, and mitigate the impact of pests and diseases on food production.Overall, the use of 5-Bromothiophene-2-carboxamide in chemical synthesis showcases its importance as a versatile and valuable building block in the development of innovative compounds with diverse applications in the fields of pharmaceuticals, agrochemicals, and specialty chemicals.