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About This Item
Linear Formula:
C6H5C6H4CHO
CAS Number:
Molecular Weight:
182.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
96%
assay
96%
refractive index
n20/D >1.6220 (lit.)
bp
91-92 °C/0.15 mmHg (lit.)
density
1.130 g/mL at 25 °C (lit.)
functional group
aldehyde, phenyl
storage temp.
2-8°C
SMILES string
O=Cc1ccccc1-c2ccccc2
InChI
1S/C13H10O/c14-10-12-8-4-5-9-13(12)11-6-2-1-3-7-11/h1-10H
InChI key
LCRCBXLHWTVPEQ-UHFFFAOYSA-N
General description
Biphenyl-2-carboxaldehyde is an oxygen-containing polycyclic aromatic hydrocarbon derivative (OPAH). It can be prepared via Suzuki cross-coupling reaction between phenyl boronic acid and 2-bromobenzaldehyde.
Application
Biphenyl-2-carboxaldehyde may be used in the preparation of 9-ethylthiofluorene.
Disclaimer
Refrigerate
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
215.6 °F - closed cup
flash_point_c
102 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Synthesis and application of ortho-palladated complex of (4-phenylbenzoylmethylene) triphenylphosphorane as a highly active catalyst in the Suzuki cross-coupling reaction.
Karami K, e tal.
Journal of Organometallic Chemistry, 696(4), 940-945 (2011)
Microbial formation and degradation of oxygen-containing polycyclic aromatic hydrocarbons (OPAHs) in soil during short-term incubation.
Wilcke W, et al.
Environmental Pollution (Barking, Essex : 1987), 184, 385-390 (2014)
The preparation of 9-alkylthiofluorenes from biphenyl-2-carboxaldehydes.
Leber JD and Elliott JD.
Tetrahedron Letters, 30(49), 6849-6850 (1989)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 400076-1MG | 04055977212303 |
| 00190585-10MG | 04061838602374 |
| 56690-1MG | 04061826672501 |
| 548049-5G | 04061832574868 |
| 548049-1G | 04061836686048 |
