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Home > Boronic Acids > 287-87-6
287-87-6 | 1H-Borole
CAS No: 287-87-6 Catalog No: AG002W5M MDL No:
Product Description
Catalog Number:
AG002W5M
Chemical Name:
1H-Borole
CAS Number:
287-87-6
Molecular Formula:
C4H5B
Molecular Weight:
63.8935
InChI:
InChI=1S/C4H4B/c1-2-4-5-3-1/h1-4H
InChI Key:
VQLAEQXQCZMULP-UHFFFAOYSA-N
SMILES:
B1C=CC=C1
Properties
Complexity:
61.7
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
63.041g/mol
Formal Charge:
0
Heavy Atom Count:
5
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
62.886g/mol
Monoisotopic Mass:
63.041g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
| Title | Journal |
|---|---|
| Oligo(borolyl)benzenes--synthesis and properties. | Chemistry (Weinheim an der Bergstrasse, Germany) 20121105 |
| Synthesis, structure, and reactivity of borole-functionalized ferrocenes. | Chemistry (Weinheim an der Bergstrasse, Germany) 20120910 |
| Synthesis, coordination behavior, and reduction chemistry of cymantrenyl-1,3-bis(2,3,4,5-tetraphenyl)borole. | Chemistry (Weinheim an der Bergstrasse, Germany) 20120702 |
| Microbial community structure elucidates performance of Glyceria maxima plant microbial fuel cell. | Applied microbiology and biotechnology 20120401 |
| An isolable radical anion based on the borole framework. | Angewandte Chemie (International ed. in English) 20120319 |
| Experimental and theoretical studies on organic D-π-A systems containing three-coordinate boron moieties as both π-donor and π-acceptor. | Chemistry (Weinheim an der Bergstrasse, Germany) 20120127 |
| Recent developments in the chemistry of antiaromatic boroles. | Chemical communications (Cambridge, England) 20111021 |
| NHC-stabilized 1-hydro-1H-borole and its nondegenerate sigmatropic isomers. | Inorganic chemistry 20110516 |
| Thiophene-fused ladder boroles with high antiaromaticity. | Journal of the American Chemical Society 20110511 |
| High-level ab initio predictions for the ionization energies and heats of formation of five-membered-ring molecules: thiophene, furan, pyrrole, 1,3-cyclopentadiene, and borole, C4H4X/C4H4X+ (X = S, O, NH, CH2, and BH). | The journal of physical chemistry. A 20110210 |
| Chemical reduction and dimerization of 1-chloro-2,3,4,5-tetraphenylborole. | Chemistry (Weinheim an der Bergstrasse, Germany) 20101025 |
| Dihydrogen activation by antiaromatic pentaarylboroles. | Journal of the American Chemical Society 20100721 |
| Synthetic, structural, photophysical and computational studies of pi-conjugated bis- and tris-1,3,2-benzodiazaboroles and related bis(boryl) dithiophenes. | Dalton transactions (Cambridge, England : 2003) 20090227 |
| Controlling accumulation of fermentation inhibitors in biorefinery recycle water using microbial fuel cells. | Biotechnology for biofuels 20090101 |
| Direct functionalization at the boron center of antiaromatic chloroborole. | Chemical communications (Cambridge, England) 20081007 |
| Organometallic building blocks with amino-substituted cyclopentadienyl and boratabenzene ligands for the synthesis of heterometallic complexes and clusters. | Dalton transactions (Cambridge, England : 2003) 20060628 |
| The role of borole in a fully conjugated electron-rich system. | Chemical communications (Cambridge, England) 20040107 |
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