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Merck
CN

D131601

2,6-二甲氧基苯甲酸

98%

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线性分子式:
(CH3O)2C6H3CO2H
化学文摘社编号:
分子量:
182.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
215-985-4
Beilstein/REAXYS Number:
2212190
MDL number:
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产品名称

2,6-二甲氧基苯甲酸, 98%

InChI key

MBIZFBDREVRUHY-UHFFFAOYSA-N

InChI

1S/C9H10O4/c1-12-6-4-3-5-7(13-2)8(6)9(10)11/h3-5H,1-2H3,(H,10,11)

SMILES string

COc1cccc(OC)c1C(O)=O

assay

98%

form

powder

mp

185-187 °C (lit.)

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pictograms

Exclamation mark

signalword

Warning

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

法规信息

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历史批次信息供参考:

分析证书(COA)

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Gustavo Portalone
Acta crystallographica. Section E, Structure reports online, 67(Pt 12), o3394-o3395 (2011-12-27)
A new crystalline form of 2,6-dimeth-oxy-benzoic acid, C(9)H(10)O(4), crystallizing in a tetra-gonal unit cell has been identified during screening for co-crystals. The asymmetric unit comprises a non-planar independent mol-ecule with a synplanar conformation of the carb-oxy group. The sterically bulky
Sandra Arrault et al.
Pest management science, 58(12), 1229-1235 (2002-12-13)
Nutrient-agar plates containing isoxaben (500 mg litre(-1)) were used to isolate isoxaben-metabolising bacteria from four European soils incubated with the herbicide under laboratory conditions. In flask experiments, inoculation of a basal salts medium containing nitrogen and [phenyl-U-14C]isoxaben with an isolate
Synthesis of aryl ketones by palladium(II)-catalyzed decarboxylative addition of benzoic acids to nitriles.
Jonas Lindh et al.
Angewandte Chemie (International ed. in English), 49(42), 7733-7737 (2010-09-15)
Serdar Durdagi et al.
Bioorganic & medicinal chemistry, 19(4), 1381-1389 (2011-02-02)
Carbonic anhydrases (CAs, EC 4.2.1.1) are inhibited by sulfonamides, inorganic anions, phenols, coumarins (acting as prodrugs) and polyamines. A novel class of CA inhibitors (CAIs), interacting with the CA isozymes I, II (cytosolic) and IX, XII (transmembrane, tumor-associated) in a

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