M13203
3-甲氧基儿茶酚
99%
别名:
1,2-二羟基-3-甲氧苯, 3-甲氧基邻苯二酚, 酚单甲醚
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关于此项目
线性分子式:
CH3OC6H3(OH)2
化学文摘社编号:
分子量:
140.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-276-4
Beilstein/REAXYS Number:
1909165
MDL number:
Assay:
99%
InChI key
LPYUENQFPVNPHY-UHFFFAOYSA-N
InChI
1S/C7H8O3/c1-10-6-4-2-3-5(8)7(6)9/h2-4,8-9H,1H3
SMILES string
COc1cccc(O)c1O
assay
99%
bp
146-147 °C/15 mmHg (lit.)
Quality Level
signalword
Warning
hcodes
Hazard Classifications
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
M Hirose et al.
Japanese journal of cancer research : Gann, 81(9), 857-861 (1990-09-01)
The effects of sodium nitrite (NaNO2) and catechol or 3-methoxycatechol in combination were examined in male F344 rats. Animals were treated with 0.3% NaNO2 in the drinking water and 0.8% catechol or 2% 3-methoxycatechol in powdered diet for 24 weeks.
M Kawabe et al.
Japanese journal of cancer research : Gann, 85(1), 17-25 (1994-01-01)
The effects of combined treatment with NaNO2 and phenolic compounds on N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) stomach carcinogenesis were investigated in F344 rats. In the first experiment, groups of 15-20 male rats were treated with an intragastric dose of 150 mg/kg body weight
Keith M Anderson et al.
The Journal of organic chemistry, 72(26), 9875-9880 (2007-11-30)
A novel universal support for deoxyribo- and ribonucleic acid synthesis has been developed. The support, constructed from 1,4-dimethoxycatechol, represents an improvement over existing universal supports because of its ability to cleave and deprotect under mild conditions in standard reagents. Because
Ying Tao et al.
Journal of bacteriology, 186(14), 4705-4713 (2004-07-03)
Wild-type toluene 4-monooxygenase (T4MO) of Pseudomonas mendocina KR1 oxidizes toluene to p-cresol (96%) and oxidizes benzene sequentially to phenol, to catechol, and to 1,2,3-trihydroxybenzene. In this study T4MO was found to oxidize o-cresol to 3-methylcatechol (91%) and methylhydroquinone (9%), to
Sam J B Mallinson et al.
Nature communications, 9(1), 2487-2487 (2018-06-29)
Microbial aromatic catabolism offers a promising approach to convert lignin, a vast source of renewable carbon, into useful products. Aryl-O-demethylation is an essential biochemical reaction to ultimately catabolize coniferyl and sinapyl lignin-derived aromatic compounds, and is often a key bottleneck
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