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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)-

Boronic acid, (5-chloro-2-thienyl)-

OB(c1ccc(s1)Cl)O Request for Quotation
Chemical Name: Boronic acid, (5-chloro-2-thienyl)-
CAS Number: 162607-18-3
Product Number: AG003MP4(AGN-PC-0KK6HY)
Synonyms:
MDL No: MFCD00236030
Molecular Formula: C4H4BClO2S
Molecular Weight: 162.4024

Identification/Properties

Properties
MP:
136-140 °C(lit.)
BP:
320.9°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
162.394g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
161.971g/mol
Monoisotopic Mass:
161.971g/mol
Topological Polar Surface Area:
68.7A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
103
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:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(5-Chlorothiophen-2-yl)boronic acid is a versatile compound commonly used in organic synthesis as a key building block in the preparation of various pharmaceuticals, agrochemicals, and materials. Its application in Suzuki-Miyaura cross-coupling reactions enables the formation of carbon-carbon bonds, facilitating the efficient construction of complex organic molecules. Additionally, this boronic acid derivative serves as a valuable reagent in the development of novel materials for electronic devices and serves as a crucial tool in the creation of advanced functional polymers. Its compatibility with a wide range of functional groups makes it a sought-after reagent in the field of chemical synthesis, allowing for intricate molecular designs and efficient access to diverse chemical structures.