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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)-

(2-chloro-5-cyanopyridin-3-yl)boronic acid

N#Cc1cnc(c(c1)B(O)O)Cl Request for Quotation
Chemical Name: (2-chloro-5-cyanopyridin-3-yl)boronic acid
CAS Number: 957060-96-7
Product Number: AG003BMR(AGN-PC-0713HI)
Synonyms:
MDL No:
Molecular Formula: C6H4BClN2O2
Molecular Weight: 182.3722

Identification/Properties

Properties
MP:
238-241℃
BP:
399.6 °C at 760 mmHg
Storage:
-10 ℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
182.37g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
182.005g/mol
Monoisotopic Mass:
182.005g/mol
Topological Polar Surface Area:
77.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
205
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P403+P233-P501
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile chemical compound that plays a crucial role in chemical synthesis processes. Specifically, it is utilized as a key building block in the creation of various functionalized molecules due to its unique structural properties. By serving as a valuable boronic acid derivative, $name$ enables the formation of complex structures through cross-coupling reactions and Suzuki-Miyaura couplings. This compound acts as a reliable reagent in organic chemistry, facilitating the efficient construction of diverse molecular structures with tailored functionalities. Furthermore, its compatibility with a wide range of reaction conditions makes it an indispensable tool for researchers and chemists seeking to synthesize novel compounds with enhanced properties.