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104736

Sigma-Aldrich

Ethyl isonicotinate

98%

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About This Item

Empirical Formula (Hill Notation):
C8H9NO2
CAS Number:
1570-45-2
Molecular Weight:
151.16
Beilstein:
122942
EC Number:
216-379-2
MDL number:
MFCD00006428
UNSPSC Code:
12352100
PubChem Substance ID:
24846672
NACRES:
NA.22

Quality Level

100

Assay

98%

refractive index

n20/D 1.501 (lit.)

bp

92 °C/8 mmHg (lit.)

density

1.009 g/mL at 25 °C (lit.)

functional group

ester

SMILES string

CCOC(=O)c1ccncc1

InChI

1S/C8H9NO2/c1-2-11-8(10)7-3-5-9-6-4-7/h3-6H,2H2,1H3

InChI key

MCRPKBUFXAKDKI-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P261 - P305 + P351 + P338

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

190.4 °F - closed cup

Flash Point(C)

88 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCB8908
BCBW6238
BCBR3908V
BCBQ0208V
BCBL4263V

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I Martin et al.
Acta chemica Scandinavica (Copenhagen, Denmark : 1989), 49(3), 230-232 (1995-03-01)
The NMDA antagonist CGS 19755 (cis-4-phosphonomethyl-2-piperidinecarboxylic acid) has been prepared by applying Minisci reaction conditions [formamide, hydrogen peroxide, iron(II) sulfate] to ethyl isonicotinate, reduction of the ester with sodium borohydride, alcoholysis of the 2-carboxamide, formation of 4-(diethylphosphonomethyl)-2-pyridinecarboxylate, hydrogenation of the
Gabriella Tamasi et al.
Journal of inorganic biochemistry, 102(10), 1874-1884 (2008-08-08)
The reaction of RuCl(3)(NO).H(2)O with 4-methylpyrimidine (MePYM) and ethylisonicotinate (EINT), in absolute ethanol at 40-55 degrees C afforded crystalline trans-[RuCl(3)(NO)L(2)] complexes. Structural studies via X-ray diffraction, and spectroscopic methods (NMR, IR, UV-visible (UV-Vis)) revealed that the molecular structures have the

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