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Propanoicacid, 2-nitro-, ethyl ester

Names

[ CAS No. ]:
2531-80-8

[ Name ]:
Propanoicacid, 2-nitro-, ethyl ester

[Synonym ]:
2-nitropropanoic acid ethyl ester
Propanoic acid,2-nitro-,ethyl ester
MFCD00024818
2-nitro-propionic acid ethyl ester
ethyl-2-nitropropionate

Chemical & Physical Properties

[ Boiling Point ]:
75ºC(9 torr)

[ Molecular Formula ]:
C5H9NO4

[ Molecular Weight ]:
147.12900

[ Flash Point ]:
89.4ºC

[ Exact Mass ]:
147.05300

[ PSA ]:
72.12000

[ LogP ]:
0.73790

[ Vapour Pressure ]:
0.519mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.421(lit.)

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

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

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NA 1993 / PGIII

[ HS Code ]:
2915900090

Precursor & DownStream

Customs

[ HS Code ]: 2915900090

[ Summary ]:
2915900090 other saturated acyclic monocarboxylic acids and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:5.5% General tariff:30.0%

Articles

5-Carboxy-5-methyl-1-pyrroline N-oxide: a spin trap for the hydroxyl radical. Tsai P, et al.

J. Chem. Soc., Perkin Trans. II 6 , 875-880, (2001)

Detection of superoxide anion using an isotopically labeled nitrone spin trap: potential biological applications.

FEBS Lett. 473(1) , 58-62, (2000)

We describe the synthesis and biological applications of a novel nitrogen-15-labeled nitrone spin trap, 5-ethoxycarbonyl-5-methyl-1-pyrroline N-oxide ([(15)N]EMPO) for detecting superoxide anion. Supe...

Structure reassignment and synthesis of Jenamidines A1/A2, synthesis of (+)-NP25302, and formal synthesis of SB-311009 analogues.

J. Org. Chem. 71(22) , 8579-90, (2006)

The proposed structures of jenamidines A, B, and C (1-3) were revised to jenamidines A1/A2, B1/B2, and C (8-10). Jenamidines A1/A2 (8) were synthesized from activated proline derivative 43 by conversi...


More Articles


Related Compounds

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