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![2′-Formyl[1,1′-biphenyl]-2-carboxylic acid AldrichCPR](/deepweb/assets/sigmaaldrich/product/structures/757/208/c9ebb62e-693f-412a-ab3c-83b3c41e44cd/640/c9ebb62e-693f-412a-ab3c-83b3c41e44cd.png)
化驗
96%
折射率
n20/D >1.6220 (lit.)
bp
91-92 °C/0.15 mmHg (lit.)
密度
1.130 g/mL at 25 °C (lit.)
官能基
aldehyde
phenyl
儲存溫度
2-8°C
SMILES 字串
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 密鑰
LCRCBXLHWTVPEQ-UHFFFAOYSA-N
一般說明
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.
應用
Biphenyl-2-carboxaldehyde may be used in the preparation of 9-ethylthiofluorene.
注意
需冷藏
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
215.6 °F - closed cup
閃點（°C）
102 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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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)
The preparation of 9-alkylthiofluorenes from biphenyl-2-carboxaldehydes.
Leber JD and Elliott JD.
Tetrahedron Letters, 30(49), 6849-6850 (1989)
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)
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