2-(2-aminoethylamino)-5-nitropyridine

Names

[ CAS No. ]:
29602-39-9

[ Name ]:
2-(2-aminoethylamino)-5-nitropyridine

[Synonym ]:
MFCD00006254
einecs 249-721-4

Chemical & Physical Properties

[ Density]:
1.358 g/cm3

[ Boiling Point ]:
382.4ºC at 760 mmHg

[ Melting Point ]:
126-128 °C(lit.)

[ Molecular Formula ]:
C₇H₁₀N₄O₂

[ Molecular Weight ]:
182.18000

[ Flash Point ]:
185ºC

[ Exact Mass ]:
182.08000

[ PSA ]:
96.76000

[ LogP ]:
1.65690

[ Vapour Pressure ]:
4.75E-06mmHg at 25°C

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

2-Chloro-5-nitropyridine
1,2-Ethanediamine

DownStream

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Alternative approaches for the detection of various phospholipid classes by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

J. Mass Spectrom. 39(4) , 412-22, (2004)

The detection of phospholipids (PLs) by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry was demonstrated nearly a decade ago. However, its use as a conventional tool for P...

A Convenient Solid Phase Synthesis of Disubstituted Guanidines. Sandanayake S, et al.

QSAR Comb. Sci. 23(8) , 655-661, (2004)

2-(2-Aminoethylamino)-5-chloropyridine
(2S)-5-amino-2-(2-aminoethylamino)-5-oxopentanoic acid
2-(2-Chlorophenoxy)-5-nitropyridine
2-(2-Fluorophenoxy)-5-nitropyridine
2-(2-Bromoethyl)-5-nitropyridine
2-(2-Bromophenoxy)-5-nitropyridine
(2R)-2-(3-phenylpropanamido)propanoic acid
N-((1-(4-fluorophenyl)cyclopropyl)methyl)benzamide
N-[(3-chlorophenyl)methyl]-N-phenyl-[1,2,4]triazolo[4,3-a]pyridine-6-sulfonamide
1-(3-methylbenzyl)-3-((4-methylpiperidin-1-yl)sulfonyl)pyridin-2(1H)-one
1-(Benzo[d][1,3]dioxol-5-yl)-3-((1-(pyridin-2-yl)piperidin-4-yl)methyl)urea
3-{[4-(4-chlorophenyl)piperazino]carbonyl}-6-isobutylisothiazolo[4,3-d]pyrimidine-5,7(4H,6H)-dione
1-(Benzo[d][1,3]dioxol-5-yl)-3-((1-(pyrimidin-2-yl)piperidin-4-yl)methyl)urea
methyl 1-(3-(4-chlorophenyl)-5-methyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidine-7-carbonyl)piperidine-4-carboxylate
N-[3-(3-Fluorophenyl)cyclobutyl]-3-methylbenzenamine
2-((1-(4-(difluoromethoxy)phenyl)-5-(3-nitrophenyl)-1H-imidazol-2-yl)thio)acetamide

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