Structure

2-Bromophenylboronic acid

CAS
244205-40-1
Catalog Number
ACM244205401
Category
Boronic Acids
Molecular Weight
200.83
Molecular Formula
C6H6BBrO2

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Specification

Synonyms
Boronic acid,B-(2-bromophenyl)-
IUPAC Name
(2-bromophenyl)boronic acid
Canonical SMILES
B(C1=CC=CC=C1Br)(O)O
InChI
InChI=1S/C6H6BBrO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4,9-10H
InChI Key
PLVCYMZAEQRYHJ-UHFFFAOYSA-N
Boiling Point
329.2±44.0 °C
Melting Point
113 °C (lit.)
Density
1.67±0.1 g/ml
Complexity
110
Covalently-Bonded Unit Count
1
Exact Mass
199.96442g/mol
Formal Charge
0
H-Bond Acceptor
2
H-Bond Donor
2
Heavy Atom Count
10
Monoisotopic Mass
199.96442g/mol
Rotatable Bond Count
1
What is the molecular formula of 2-Bromophenylboronic acid?

The molecular formula of 2-Bromophenylboronic acid is C6H6BBrO2.

What is the molecular weight of 2-Bromophenylboronic acid?

The molecular weight of 2-Bromophenylboronic acid is 200.83 g/mol.

What is the IUPAC name of 2-Bromophenylboronic acid?

The IUPAC name of 2-Bromophenylboronic acid is (2-bromophenyl)boronic acid.

What is the InChI of 2-Bromophenylboronic acid?

The InChI of 2-Bromophenylboronic acid is InChI=1S/C6H6BBrO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4,9-10H.

What is the InChIKey of 2-Bromophenylboronic acid?

The InChIKey of 2-Bromophenylboronic acid is PLVCYMZAEQRYHJ-UHFFFAOYSA-N.

What is the canonical SMILES of 2-Bromophenylboronic acid?

The canonical SMILES of 2-Bromophenylboronic acid is B(C1=CC=CC=C1Br)(O)O.

What is the CAS number of 2-Bromophenylboronic acid?

The CAS number of 2-Bromophenylboronic acid is 244205-40-1.

What is the EC number of 2-Bromophenylboronic acid?

The EC number of 2-Bromophenylboronic acid is 678-199-4.

Is 2-Bromophenylboronic acid a covalently-bonded unit?

Yes, 2-Bromophenylboronic acid is a covalently-bonded unit with a count of 1.

Downstream Synthesis Route 1

  • 62-53-3
  • 244205-40-1
  • 61613-22-7

Reference: [1]Journal of Organic Chemistry,2006,vol. 71,p. 9522 - 9524

Downstream Synthesis Route 2

  • 244205-40-1
  • 354574-31-5
  • 4544-87-0

Reference: [1]Noguchi, Hiroyoshi; Hojo, Kosho; Suginome, Michinori [Journal of the American Chemical Society, 2007, vol. 129, # 4, p. 758 - 759]

Downstream Synthesis Route 3

  • 244205-40-1
  • 1628-29-1

Reference: [1] Chemistry Letters, 2018, vol. 47, # 7, p. 825 - 828

Downstream Synthesis Route 4

  • 244205-40-1
  • 16567-18-3

Reference: [1] Chinese Chemical Letters, 2014, vol. 25, # 5, p. 779 - 782

Downstream Synthesis Route 5

  • 244205-40-1
  • 3652-89-9

Reference: [1] Journal of the American Chemical Society, 2011, vol. 133, # 35, p. 13872 - 13875

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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