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质量水平
检测方案
98%
mp
179-182 °C (lit.)
SMILES字符串
Oc1ccc(C=O)c2ccccc12
InChI
1S/C11H8O2/c12-7-8-5-6-11(13)10-4-2-1-3-9(8)10/h1-7,13H
InChI key
LORPDGZOLAPNHP-UHFFFAOYSA-N
应用
4-Hydroxy-1-naphthaldehyde was used in the preparation of racemic 1- and 2-naphthol analogues of tyrosine, 2-amino-3-(4-hydroxy-1-naphthyl)propanoic acid hydrochloride and 2-amino-3-(6-hydroxy-2-naphthyl)propanoic acid hydrobromide.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Syntheses of 1-and 2-naphthol analogs of DL-tyrosine. Potential fluorescent probes of peptide structure and dynamics in complex environments.
Vela MA, et al.
The Journal of Organic Chemistry, 55(9), 2913-2918 (1990)
Zi-Jian Chen et al.
Ecotoxicology and environmental safety, 196, 110533-110533 (2020-04-05)
1-naphthol (1-NAP) is the main metabolite of pesticide carbaryl and naphthalene, and is also a genotoxic and carcinogenic intermediate in the synthesis of organic compound, dyes, pigment and pharmaceutical industry. In this work, two novel haptens were designed and synthesized
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