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About This Item
线性分子式:
CH3C10H6CO2H
CAS号:
分子量:
186.21
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
97%
mp
179-181 °C (lit.)
官能团
carboxylic acid
SMILES字符串
Cc1ccc(C(O)=O)c2ccccc12
InChI
1S/C12H10O2/c1-8-6-7-11(12(13)14)10-5-3-2-4-9(8)10/h2-7H,1H3,(H,13,14)
InChI key
SIVYRLBDAPKADZ-UHFFFAOYSA-N
一般描述
4-Methyl-1-naphthoic acid is a naphthoic acid derivative
应用
4-Methyl-1-naphthoic acid may be used to synthesize:
- 2-methyl-1-propyl-3-(4-methyl-1-naphthoyl)indole, JWH-148
- 4-methyl-1-naphthylcarbinol
- 1,4-dioxan-2-yl 4-methyl-1-naphthoate
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Jincan Zhao et al.
The Journal of organic chemistry, 79(9), 3847-3855 (2014-04-15)
An iron-catalyzed oxidative esterification reaction between unactivated C(sp(3))-H bonds from symmetric and asymmetric ethers and carboxylic acids using di-tert-butyl peroxide (DTBP) as the oxidant via a cross dehydrogenative coupling (CDC) reaction was established, which tolerates a wide range of cyclic
John W Huffman et al.
Bioorganic & medicinal chemistry, 13(1), 89-112 (2004-12-08)
In an effort to improve indole-based CB(2) cannabinoid receptor ligands and also to develop SAR for both the CB(1) and CB(2) receptors, 47 indole derivatives were prepared and their CB(1) and CB(2) receptor affinities were determined. The indole derivatives include
Preparation of a series of substituted fluoromethylnaphthalenes.
Dixon EA, et al.
Canadian Journal of Chemistry, 59(17), 2629-2641 (1981)
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