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88982-39-2

88982-39-2 | Boronic acid, 2-propenyl-

CAS No: 88982-39-2 Catalog No: AG00IFJ2 MDL No:

Product Description

Catalog Number:
AG00IFJ2
Chemical Name:
Boronic acid, 2-propenyl-
CAS Number:
88982-39-2
IUPAC Name:
prop-2-enylboronic acid
InChI:
InChI=1S/C3H7BO2/c1-2-3-4(5)6/h2,5-6H,1,3H2
InChI Key:
QGLVEAGMVUQOJP-UHFFFAOYSA-N

Properties

Complexity:
44.1  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
86.054g/mol
Formal Charge:
0
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
85.897g/mol
Monoisotopic Mass:
86.054g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
40.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0

Literature

Title Journal
Facile preparation of allylzinc species from allylboronates and zinc amide via a boron-to-zinc exchange process and their reactions with carbonyl compounds, imines and hydrazones. Chemical communications (Cambridge, England) 20121025
'Design' of boron-based compounds as pro-nucleophiles and co-catalysts for indium(I)-catalyzed allyl transfer to various Csp3-type electrophiles. Chemistry, an Asian journal 20110905
Ni(0)-catalyzed 1,4-selective diboration of conjugated dienes. Organic letters 20101001
Chiral Brønsted acid-catalyzed allylboration of aldehydes. Journal of the American Chemical Society 20100901
Regio- and stereoselective Ni-catalyzed 1,4-hydroboration of 1,3-dienes: access to stereodefined (Z)-allylboron reagents and derived allylic alcohols. Journal of the American Chemical Society 20100303
Quantum chemical study of Lewis acid catalyzed allylboration of aldehydes. Journal of the American Chemical Society 20080917
Part 3. Triethylborane-air: a suitable initiator for intermolecular radical additions of S-2-oxoalkyl-thionocarbonates (S-xanthates) to olefins. Beilstein journal of organic chemistry 20070101
Brønsted acid-catalyzed allylboration: short and stereodivergent synthesis of all four eupomatilone diastereomers with crystallographic assignments. Journal of the American Chemical Society 20050921
Quantum chemical study on asymmetric allylation of benzaldehyde in the presence of chiral allylboronate. Journal of Zhejiang University. Science. B 20050601
Pd-catalyzed cross-coupling of Baylis-Hillman acetate adducts with bis(pinacolato)diboron: an efficient route to functionalized allyl borates. The Journal of organic chemistry 20040820
Catalytic enantioselective allylboration of ketones. Journal of the American Chemical Society 20040728
Palladium-catalyzed coupling of allyl acetates with aldehyde and imine electrophiles in the presence of Bis(pinacolato)diboron. Organic letters 20030821
Dramatic rate enhancement with preservation of stereospecificity in the first metal-catalyzed additions of allylboronates. Journal of the American Chemical Society 20021002
Secondary deuterium kinetic isotope effects in irreversible additions of allyl reagents to benzaldehyde. The Journal of organic chemistry 20020614

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