质量水平
方案
96%
表单
powder
沸点
300 °C (lit.)
mp
157-160 °C (lit.)
SMILES字符串
OC(=O)c1cccc2ccccc12
InChI
1S/C11H8O2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,(H,12,13)
InChI key
LNETULKMXZVUST-UHFFFAOYSA-N
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应用
1-萘甲酸可作为以下应用的反应剂：
- 在铑催化剂存在下，与炔烃通过脱水环化反应制备萘嵌苯酮。
- 使用Rh催化剂，与2-丁炔通过有氧的氧化环化反应制备异香豆素衍生物。
- 与N,O-二甲基羟胺和三氯化磷反应制备N-甲氧基-N-甲基-1-萘甲酰胺（Weinreb酰胺）。
- 通过Birch还原反应制备1,4-二氢-1-萘羧酸。
其他说明
残留物为 2-萘甲酸
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
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Mutual activation: Suzuki-Miyaura coupling through direct cleavage of the sp2 C-O bond of naphtholate.
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A method is described for converting tert-butyl benzoates or tert-butyl 1-naphthoates into derivatives having an alkyl or substituted alkyl group in a 1,4-relationship to an alkyl, aryl, alkenyl, or alkynyl group. Key steps in the sequence are (i) addition of
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Spray-dried particles (SDPs) with indomethacin (IND) and alpha-glycosyl transferase-treated stevia (Stevia-G) indicated extremely high dissolution rates and apparent solubility compared to particles of a ground mixture and a physical mixture of IND/Stevia-G. The apparent solubility of IND from SDPs was
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