Home Halogens Borane, dichlorophenyl-

Borane, dichlorophenyl-

CAS No.:
873-51-8
Catalog Number:
AG004HGH
Molecular Formula:
C6H5BCl2
Molecular Weight:
158.8209
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Purity
Availability
Location
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5g
>98.0%(T)
1 week
United States
$217
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Product Description
Catalog Number:
AG004HGH
Chemical Name:
Borane, dichlorophenyl-
CAS Number:
873-51-8
Molecular Formula:
C6H5BCl2
Molecular Weight:
158.8209
MDL Number:
MFCD00013612
IUPAC Name:
dichloro(phenyl)borane
InChI:
InChI=1S/C6H5BCl2/c8-7(9)6-4-2-1-3-5-6/h1-5H
InChI Key:
NCQDQONETMHUMY-UHFFFAOYSA-N
SMILES:
ClB(c1ccccc1)Cl
NSC Number:
93889
Properties
Complexity:
79.1  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
157.986g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
158.816g/mol
Monoisotopic Mass:
157.986g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
Title Journal
Ring cleavage reactions of methyl α-D-allopyranoside derivatives with phenylboron dichloride and triethylsilane. Molecules (Basel, Switzerland) 20111213
New azaborine-thiophene heteroacenes. Chemical communications (Cambridge, England) 20101007
Dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine-dichlorophenylborane. Acta crystallographica. Section E, Structure reports online 20091101
Reluctance of 4-chloro-5-metalla-1,3,2-diazaborolines to undergo metal halide beta-elimination: an opportunity for C-functionalization of 1,3,2-diazaborolines. Inorganic chemistry 20081103
Single-boron complexes of N-confused and N-fused porphyrins. Inorganic chemistry 20070820
Lewis acid mediated reactions of aldehydes with styrene derivatives: synthesis of 1,3-dihalo-1,3-diarylpropanes and 3-chloro-1,3-diarylpropanols. The Journal of organic chemistry 20051209
Synthesis of a new N-acetyl thiazolidinethione reagent and its application to a highly selective asymmetric acetate aldol reaction. Organic letters 20040902
Highly selective asymmetric acetate aldol reactions of an N-acetyl thiazolidinethione reagent. Organic letters 20040108
Properties