3,5-Dibromobenzaldehyde
Product Information
Molecular Formula
C7H4Br2O
Molecular Weight
263.91
Description
3,5-Dibromobenzaldehyde (CAS# 56990-02-4) is a dibrominated benzaldehyde that is a very useful building block for the preparation of a wide range of biologically active compounds such as a antibacterials.
Synonyms
3,5-dibromobenzaldehyde
IUPAC Name
3,5-dibromobenzaldehyde
SMILES
C1=C(C=C(C=C1Br)Br)C=O
InChI
InChI=1S/C7H4Br2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H
InChI Key
ZLDMZIXUGCGKMB-UHFFFAOYSA-N
Boiling Point
287.221 °C at 760 mmHg
Melting Point
84-88 °C
Purity
> 97.0 % (GC)
Density
1.977 g/cm3
Appearance
White powder
LogP
3.02410
Safety Information
Hazards
H314
Precautionary Statement
P260, P264, P280, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P332+P313, P337+P313, P362, P363, P405, and P501
Signal Word
Danger
Computed Properties
XLogP3
2.8
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
1
Exact Mass
263.86084 g/mol
Monoisotopic Mass
261.86289 g/mol
Topological Polar Surface Area
17.1Ų
Heavy Atom Count
10
Formal Charge
0
Complexity
117
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 |
|---|---|---|
| CN-113549062-A | Chiral quaternary ammonium salt phase transfer catalyst with high steric hindrance derived from cinchona alkaloid and synthesis method thereof | 2021-08-20 |
| CN-113318707-A | Organic supermolecule gel system of binuclear rhodium-porphyrin derivative and preparation method thereof | 2021-06-11 |
| CN-113336622-A | Fluorene derivative with AIE characteristic, preparation method and application | 2021-04-09 |
| US-11045792-B1 | Highly efficient nanosized mesoporous CuMgAl ternary oxide catalyst | 2020-09-30 |
| CN-111875599-A | Y-type co-sensitizer with rhodanine acetic acid as receptor and preparation method thereof | 2020-08-12 |
| CN-111892583-A | Y-type co-sensitizer with cyanoacetic acid as receptor and preparation method thereof | 2020-08-12 |
| US-2022040108-A1 | Light upconversion silica particles | 2020-08-07 |
| US-2022040683-A1 | Surface-modified light upconversion silica particles | 2020-08-07 |
| US-2022041925-A1 | Light upconversion microcapsule shells | 2020-08-07 |
| CN-111840282-A | Application of thiobenzimidazolone Schiff base in inhibition of tyrosinase activity | 2020-08-05 |
