526533
4-Methyl-1-naphthoic acid
97%
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About This Item
Fórmula lineal:
CH3C10H6CO2H
Número de CAS:
Peso molecular:
186.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
97%
mp
179-181 °C (lit.)
functional group
carboxylic acid
SMILES string
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
General description
4-Methyl-1-naphthoic acid is a naphthoic acid derivative
Application
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
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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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