1. Home
  2. 1,3,2-Dioxaborolane,4,4,5,5-tetramethyl-2-(2-methyl-5-nitrophenyl)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

1,3,2-Dioxaborolane,4,4,5,5-tetramethyl-2-(2-methyl-5-nitrophenyl)-

CC1(C)OB(OC1(C)C)c1cc(ccc1C)[N+](=O)[O-] Request for Quotation
Chemical Name: 1,3,2-Dioxaborolane,4,4,5,5-tetramethyl-2-(2-methyl-5-nitrophenyl)-
CAS Number: 957062-84-9
Product Number: AG003HNS(AGN-PC-0W5BBR)
Synonyms:
MDL No:
Molecular Formula: C13H18BNO4
Molecular Weight: 263.0973

Identification/Properties

Properties
BP:
378.9°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
263.1g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
263.133g/mol
Monoisotopic Mass:
263.133g/mol
Topological Polar Surface Area:
64.3A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
350
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Methyl-5-nitrophenylboronic Acid Pinacol Ester is a valuable compound widely used in chemical synthesis as a versatile building block. This compound is particularly useful in the field of organic chemistry for its ability to react with various electrophiles and nucleophiles to form complex molecules with specific functionalities. Its application in Suzuki-Miyaura cross-coupling reactions is noteworthy, where it serves as a key reagent for the formation of carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and materials. Furthermore, 2-Methyl-5-nitrophenylboronic Acid Pinacol Ester is utilized in the preparation of heterocyclic compounds, natural product synthesis, and the development of new materials with tailored properties.The unique reactivity of this compound allows chemists to access a diverse range of molecular structures, making it a valuable tool in the repertoire of synthetic chemists. Its compatibility with a variety of functional groups and reaction conditions further enhances its utility in the construction of complex organic molecules.In summary, 2-Methyl-5-nitrophenylboronic Acid Pinacol Ester plays a crucial role in modern chemical synthesis by enabling the efficient and selective formation of carbon-carbon bonds, thus facilitating the creation of novel compounds with potential applications in various fields.