推薦產品
化驗
97%
mp
179-181 °C (lit.)
SMILES 字串
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 密鑰
SIVYRLBDAPKADZ-UHFFFAOYSA-N
一般說明
4-Methyl-1-naphthoic acid is a naphthoic acid derivative
應用
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
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號，寫有 ‘Lot’或‘Batch’.。
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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