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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)-

Vinylboronic acid MIDA ester

C=CB1OC(=O)CN(CC(=O)O1)C Request for Quotation
Chemical Name: Vinylboronic acid MIDA ester
CAS Number: 1104636-73-8
Product Number: AG003NAB(AGN-PC-0WAFGW)
Synonyms:
MDL No:
Molecular Formula: C7H10BNO4
Molecular Weight: 182.9696

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
182.97g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
183.07g/mol
Monoisotopic Mass:
183.07g/mol
Topological Polar Surface Area:
55.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
223
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Vinylboronic acid MIDA ester is a versatile molecule that finds widespread application in organic synthesis. This compound serves as a valuable building block due to its ability to undergo various transformations, making it an essential tool for chemists in the laboratory. In chemical synthesis, Vinylboronic acid MIDA ester plays a crucial role in Suzuki-Miyaura cross-coupling reactions, allowing for the efficient construction of carbon-carbon bonds. Furthermore, it can also be utilized in the functionalization of alkenes and alkynes, enabling the introduction of diverse functional groups with high regio- and stereo-selectivity. Additionally, Vinylboronic acid MIDA ester exhibits excellent stability under a wide range of reaction conditions, making it particularly useful for complex multistep synthetic sequences. Overall, the unique properties and reactivity of Vinylboronic acid MIDA ester make it an indispensable tool for synthetic chemists seeking to access diverse and complex molecular architectures.