D131601
2,6-Dimethoxybenzoic acid
98%
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About This Item
Linear Formula:
(CH3O)2C6H3CO2H
CAS Number:
Molecular Weight:
182.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
215-985-4
Beilstein/REAXYS Number:
2212190
MDL number:
Product Name
2,6-Dimethoxybenzoic acid, 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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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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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