252794
3-羟基苯甲酸甲酯
99%
别名:
3-(Methoxycarbonyl)phenol, 3-Carbomethoxyphenol, 3-Hydroxybenzoic acid methyl ester, Methyl m-hydroxybenzoate, m-Carbomethoxyphenol, m-Hydroxybenzoic acid methyl ester
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关于此项目
线性分子式:
HOC6H4CO2CH3
化学文摘社编号:
分子量:
152.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
243-071-5
Beilstein/REAXYS Number:
2208129
MDL number:
产品名称
3-羟基苯甲酸甲酯, 99%
InChI key
YKUCHDXIBAQWSF-UHFFFAOYSA-N
InChI
1S/C8H8O3/c1-11-8(10)6-3-2-4-7(9)5-6/h2-5,9H,1H3
SMILES string
COC(=O)c1cccc(O)c1
assay
99%
form
solid
bp
280-281 °C/709 mmHg (lit.)
mp
70-72 °C (lit.)
functional group
ester
Quality Level
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Application
Methyl 3-hydroxybenzoate has been used in synthesis of:
- 3-hydroxybenzene-1,2-dicarbaldehyde
- O-methyl O-[3-methyl-4-(methylthio)phenyl]O-(3-methylcarboxyphenyl) phosphorothioate
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Investigation of the effect of hapten heterology on immunoassay sensitivity and development of an enzyme-linked immunosorbent assay for the organophosphorus insecticide fenthion.
Kim YJ, et al.
Analytica Chimica Acta, 94(1, 29-40 (2003)
T Sakata et al.
Bioscience, biotechnology, and biochemistry, 65(10), 2315-2317 (2002-01-05)
The structure of a novel aromatic compound contained in the unidentified Rhizoglyhus mite (Acaridae: Astigmata) was elucidated, without its isolation, to be 3-hydroxybenzene-1,2-dicarbaldehyde (tentatively named gamma-acaridial) by a combination of GC/MS and GC/FT-IR together with knowledge of related mite compounds.
Deze Kong et al.
Science advances, 6(44) (2020-11-01)
Chalcone synthase (CHS) canonically catalyzes carbon-carbon bond formation through iterative decarboxylative Claisen condensation. Here, we characterize a previously unidentified biosynthetic capability of SlCHS to catalyze nitrogen-carbon bond formation, leading to the production of a hydroxycinnamic acid amide (HCAA) compound. By
Shota Machida et al.
Molecules (Basel, Switzerland), 24(23) (2019-12-01)
Twenty-one natural and unnatural phenolic compounds containing a carbohydrate moiety were synthesized and their structure-activity relationship (SAR) was evaluated for α-glucosidase inhibition and antioxidative activity. Varying the position of the galloyl unit on the 1,5-anhydro-d-glucitol (1,5-AG) core resulted in changes
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