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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:
Molecular Weight:
192.00
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Pricing and availability is not currently available.

Quality Level

assay

98%

form

solid

mp

209-212 °C (lit.)

functional group

carboxylic acid
chloro

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

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1 of 4

This Item
543918755214153281
assay

98%

assay

97%

assay

95%

assay

97%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

mp

209-212 °C (lit.)

mp

246 °C (dec.) (lit.)

mp

295-304 °C

mp

>300 °C (lit.)

form

solid

form

-

form

solid

form

-

functional group

carboxylic acid

functional group

carboxylic acid, chloro

functional group

carboxylic acid, chloro

functional group

carboxylic acid

pictograms

Exclamation mark

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


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    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
    The preparation of pyridine-4-carboxylic acid and of piperidine-4-carboxylic acid by catalytic reduction of 2, 6-dichloropyridine-4-carboxylic acid.
    Wibaut JP.
    Rec. Trav. Chim., 63(7), 141-146 (1944)
    J M Manners et al.
    Plant molecular biology, 38(6), 1071-1080 (1998-12-30)
    The plant defensin PDF1.2 has previously been shown to accumulate systemically via a salicylic acid-independent pathway in leaves of Arabidopsis upon challenge by fungal pathogens. To further investigate the signalling and transcriptional processes underlying plant defensin induction, a DNA fragment
    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
    European Journal of Organic Chemistry, 22, 4445-4449 (2003)

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