5-Bromopentylboronic acid
Product Information
Molecular Formula
C5H12BBrO2
Molecular Weight
194.9
Description
May contain various amounts of anhydride
Synonyms
5-bromopentylboronicacid; 5-BROMOPENTYLBORONICACID; 120986-85-8; (5-Bromopentyl)boronicacid; C5H12BBrO2; ACMC-1BZ87
IUPAC Name
5-bromopentylboronic acid
SMILES
B(CCCCCBr)(O)O
InChI
InChI=1S/C5H12BBrO2/c7-5-3-1-2-4-6(8)9/h8-9H,1-5H2
InChI Key
RCBNHBWNONFWHR-UHFFFAOYSA-N
Melting Point
91-96°C
Purity
95%
Appearance
White to tan solid
Storage
2-8°C
Safety Information
Hazards
H315-H319-H335
Precautionary Statement
P261-P305 + P351 + P338
Computed Properties
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
5
Exact Mass
194.01137 g/mol
Monoisotopic Mass
194.01137 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
9
Formal Charge
0
Complexity
60.9
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
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| JP-2022021687-A | Method for Producing N-Substituted (Meta) Acrylamide | 2020-07-22 |
| US-2015075789-A1 | Boronated Biopolymer Crosslinking Agents and Methods Relating Thereto | 2013-07-01 |
| US-9688906-B2 | Boronated biopolymer crosslinking agents and methods relating thereto | 2013-07-01 |
| WO-2015002669-A1 | Boronated biopolymer crosslinking agents and methods relating thereto | 2013-07-01 |
| US-2011201806-A1 | Methods for Forming Protected Organoboronic Acids | 2010-02-18 |
| US-2014073785-A1 | Methods for Forming Protected Organoboronic Acids | 2010-02-18 |
| US-2016376292-A1 | Methods for forming protected organoboronic acids | 2010-02-18 |
| US-8557980-B2 | Methods for forming protected organoboronic acids | 2010-02-18 |
| US-9353131-B2 | Methods for forming protected organoboronic acids | 2010-02-18 |
| US-9908900-B2 | Methods for forming protected organoboronic acids | 2010-02-18 |