1. Home
  2. Boronic acid, (5-methyl-2-thienyl)-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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-methyl-2-thienyl)-

OB(c1ccc(s1)C)O Request for Quotation
Chemical Name: Boronic acid, (5-methyl-2-thienyl)-
CAS Number: 162607-20-7
Product Number: AG0034AY(AGN-PC-0KK6J6)
Synonyms:
MDL No:
Molecular Formula: C5H7BO2S
Molecular Weight: 141.9839

Identification/Properties

Properties
MP:
161.5-166.5 °C(lit.)
BP:
302.9°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
141.979g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
142.026g/mol
Monoisotopic Mass:
142.026g/mol
Topological Polar Surface Area:
68.7A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
99
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


5-Methylthiophene-2-Boronic Acid, a versatile building block in chemical synthesis, is a highly valuable compound that finds widespread application in organic chemistry. With its distinct structural features, this compound serves as a crucial reagent in various synthetic processes, offering a range of possibilities for the creation of novel molecules and pharmaceuticals.One of the primary applications of 5-Methylthiophene-2-Boronic Acid lies in its role as a key intermediate in the synthesis of complex organic molecules. By participating in cross-coupling reactions, this compound enables the formation of carbon-carbon bonds, a fundamental step in the construction of intricate organic frameworks. This ability makes it a valuable tool for medicinal chemists and researchers involved in drug discovery, allowing them to access unique chemical structures that may exhibit desirable biological properties.Furthermore, 5-Methylthiophene-2-Boronic Acid serves as a critical component in the development of functional materials and agrochemicals. Its reactivity and compatibility with various reaction conditions make it a sought-after reagent for the preparation of advanced materials with tailored properties. From light-emitting diodes to crop protection agents, the versatility of this compound opens up avenues for innovation in multiple fields.In conclusion, 5-Methylthiophene-2-Boronic Acid stands out as a pivotal building block in chemical synthesis, offering chemists a versatile tool to explore new synthetic pathways and create valuable molecules with diverse applications.