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
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
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...