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D131601

Sigma-Aldrich

2,6-Dimethoxybenzoic acid

98%

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About This Item

Linear Formula:
(CH3O)2C6H3CO2H
CAS Number:
1466-76-8
Molecular Weight:
182.17
Beilstein:
2212190
EC Number:
215-985-4
MDL number:
MFCD00002437
UNSPSC Code:
12352100
PubChem Substance ID:
24893413
NACRES:
NA.22

Assay

98%

form

powder

mp

185-187 °C (lit.)

SMILES string

COc1cccc(OC)c1C(O)=O

InChI

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

InChI key

MBIZFBDREVRUHY-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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