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703966

Sigma-Aldrich

3-Bromopyridine-2-carbonitrile

97%

Synonym(s):

3-Bromo-2-cyanopyridine

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About This Item

Empirical Formula (Hill Notation):
C6H3BrN2
CAS Number:
Molecular Weight:
183.01
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level

Assay

97%

form

powder

mp

93-98 °C

functional group

bromo
nitrile

SMILES string

Brc1cccnc1C#N

InChI

1S/C6H3BrN2/c7-5-2-1-3-9-6(5)4-8/h1-3H

InChI key

HCOPIUVJCIZALB-UHFFFAOYSA-N

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This Item
662720755028759600
assay

97%

assay

97%

assay

97%

assay

95%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

form

powder

form

solid

form

solid

form

solid

mp

93-98 °C

mp

-

mp

95-100 °C

mp

250-260 °C

functional group

bromo

functional group

bromo

functional group

bromo, fluoro, nitrile

functional group

nitrile

Pictograms

Skull and crossbonesCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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S C Perricone et al.
Journal of medicinal chemistry, 37(22), 3693-3700 (1994-10-28)
Random screening identified N,N'-dicyclohexyl-4-morpholinecarboxamidine (U-18177, 1) as an orally effective nonkaliuretic diuretic in rats. The diuretic profile of 1 and its 1-adamantyl analog (U-37883A, 4) was confirmed orally in dogs, when they were less potent than standard diuretics but showed
Earl R Kern et al.
Antimicrobial agents and chemotherapy, 46(4), 991-995 (2002-03-19)
The nucleotide phosphonates cidofovir (CDV) and cyclic cidofovir (cCDV) are potent antiviral compounds when administered parenterally but are not well absorbed orally. These compounds have been reported to have activity against orthopoxvirus replication in vitro and in animal models when
Yuji Kamata et al.
Hypertension research : official journal of the Japanese Society of Hypertension, 32(3), 220-226 (2009-03-06)
It is suggested that an ATP-sensitive potassium channel blocker suppresses sodium-induced hypertension through increased secretion of urinary kallikrein. We reported that glibenclamide, an ATP-sensitive potassium channel blocker, accelerated dose-dependent secretion of renal kallikrein in sliced kidney cortex and in vivo

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