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456543

Sigma-Aldrich

2,6-Dichloropyridine-4-carboxylic acid

98%

Synonym(s):

2,6-Dichloroisonicotinic acid

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About This Item

Empirical Formula (Hill Notation):
C6H3Cl2NO2
CAS Number:
5398-44-7
Molecular Weight:
192.00
MDL number:
MFCD00234147
UNSPSC Code:
12352100
PubChem Substance ID:
24869197
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

mp

209-212 °C (lit.)

SMILES string

OC(=O)c1cc(Cl)nc(Cl)c1

InChI

1S/C6H3Cl2NO2/c7-4-1-3(6(10)11)2-5(8)9-4/h1-2H,(H,10,11)

InChI key

SQSYNRCXIZHKAI-UHFFFAOYSA-N

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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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European Journal of Organic Chemistry, 22, 4445-4449 (2003)
A Guo et al.
The Plant journal : for cell and molecular biology, 15(5), 647-656 (1998-10-21)
A clone encoding a putative soluble epoxide hydrolase (EH-1), an enzyme which converts epoxides to diols, was isolated by differential screening of a cDNA library prepared from tobacco mosaic virus (TMV)-infected tobacco leaves. To confirm that EH-1 encodes an epoxide
Uwe Conrath et al.
Trends in plant science, 7(5), 210-216 (2002-05-07)
Plants can acquire enhanced resistance to pathogens after treatment with necrotizing attackers, nonpathogenic root-colonizing pseudomonads, salicylic acid, beta-aminobutyric acid and many other natural or synthetic compounds. The induced resistance is often associated with an enhanced capacity to mobilize infection-induced cellular
Proton Mobility in 2-Substituted 1, 3-Dichlorobenzenes:?ortho? or ?meta? Metalation?
Schlosser M, et al.
European Journal of Organic Chemistry, 19, 4398-4404 (2006)
Michael Dalgaard Mikkelsen et al.
Plant physiology, 131(1), 298-308 (2003-01-17)
Glucosinolates are natural plant products that function in the defense toward herbivores and pathogens. Plant defense is regulated by multiple signal transduction pathways in which salicylic acid (SA), jasmonic acid, and ethylene function as signaling molecules. Glucosinolate content was analyzed
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