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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)-

4H-Thieno[3,2-b]pyrrole-5-carboxylic acid, 3-bromo-

OC(=O)c1cc2c([nH]1)c(cs2)Br Request for Quotation
Chemical Name: 4H-Thieno[3,2-b]pyrrole-5-carboxylic acid, 3-bromo-
CAS Number: 332099-36-2
Product Number: AG00BYH1(AGN-PC-03T74K)
Synonyms:
MDL No:
Molecular Formula: C7H4BrNO2S
Molecular Weight: 246.0812

Identification/Properties

Properties
BP:
487.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
246.078g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
244.915g/mol
Monoisotopic Mass:
244.915g/mol
Topological Polar Surface Area:
81.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
214
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Bromo-4H-thieno[3,2-b]pyrrole-5-carboxylic acid, often referred to as $name$, is a versatile compound widely utilized in chemical synthesis. Its unique structure and properties make it a valuable building block for the creation of various organic compounds.In chemical synthesis, $name$ is commonly employed as a key intermediate in the synthesis of complex organic molecules. Its functional groups, including the bromo and carboxylic acid moieties, enable facile manipulation through various chemical reactions such as nucleophilic substitution, esterification, and coupling reactions. This makes $name$ a valuable tool for the modification and functionalization of organic molecules in the synthesis of pharmaceuticals, agrochemicals, and materials.Furthermore, the presence of the thieno[3,2-b]pyrrole core in $name$ imparts unique electronic and structural properties to the compounds synthesized from it. These properties can be leveraged to design and develop new functional materials with applications in organic electronics, optoelectronics, and other advanced technologies.Overall, the versatility and reactivity of 3-Bromo-4H-thieno[3,2-b]pyrrole-5-carboxylic acid make it a valuable component in the toolkit of synthetic chemists for the efficient construction of complex organic molecules with tailored properties and functionalities.