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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)-

(5-formyl-3-methylthiophen-2-yl)boronic acid

O=Cc1cc(c(s1)B(O)O)C Request for Quotation
Chemical Name: (5-formyl-3-methylthiophen-2-yl)boronic acid
CAS Number: 1072952-28-3
Product Number: AG003BY3(AGN-PC-07XU0S)
Synonyms:
MDL No:
Molecular Formula: C6H7BO3S
Molecular Weight: 169.9940

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
169.989g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
170.021g/mol
Monoisotopic Mass:
170.021g/mol
Topological Polar Surface Area:
85.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(5-Formyl-3-methylthiophen-2-yl)boronic acid is a versatile compound commonly used in chemical synthesis as a key building block. Its boronic acid functionality allows for efficient and selective cross-coupling reactions with various organic substrates, such as aryl halides, to form complex molecular structures. This compound is particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and materials due to its ability to introduce the 5-formyl-3-methylthiophen-2-yl moiety into target molecules with precision and control. Furthermore, its unique electronic and steric properties make it a valuable tool for accessing diverse chemical space in the development of novel compounds with desired properties.