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Merck
CN

456543

2,6-二氯吡啶-4-羧酸

98%

别名:

2,6-二氯异烟酸

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关于此项目

经验公式(希尔记法):
C6H3Cl2NO2
化学文摘社编号:
分子量:
192.00
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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产品名称

2,6-二氯吡啶-4-羧酸, 98%

InChI

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

SMILES string

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

InChI key

SQSYNRCXIZHKAI-UHFFFAOYSA-N

assay

98%

form

solid

mp

209-212 °C (lit.)

functional group

carboxylic acid
chloro

Quality Level

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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


历史批次信息供参考:

分析证书(COA)

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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
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)
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
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
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

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