Ethyl cyanoglyoxylate-2-oxime

Names

[ Name ]:
Ethyl cyanoglyoxylate-2-oxime

[Synonym ]:
OxiMa
Ethyl isonitrosocyanoacetate
EINECS 223-351-3
Ethyl cyanoximidoacetate
Ethyl Cyano(hydroxyimino)acetate
Acetic acid, 2-cyano-2-(hydroxyimino)-, ethyl ester, (2E)-
ETHYL OXIMINOCYANOACETATE
ETHYL CYANOGLYOXYLATE OXIME
ETHYL CYANOGLYOXALATE-2-OXIME
Ethyl Cyanoglyoxylate-2-Oxime
Cyano(hydroxyimino)acetic Acid Ethyl Ester
Ethyl (Hydroxyimino)cyanoacetate
Oxyma Pure
Ethyl (2E)-cyano(hydroxyimino)acetate
2-Ethyloximinocyanocaetate
Ethyl Cyanoglyoxalate Oxime
MFCD00002112

Biological Activity

[Description]:

Ethyl 2-cyano-2-hydroxyiminoacetate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

[In Vitro]

高效偶联添加剂，是HOBt的更安全、不爆炸的替代品。

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
248.9±23.0 °C at 760 mmHg

[ Melting Point ]:
130-132 °C(lit.)

[ Molecular Formula ]:
C₅H₆N₂O₃

[ Molecular Weight ]:
142.11

[ Flash Point ]:
104.3±22.6 °C

[ Exact Mass ]:
142.037842

[ PSA ]:
82.68000

[ LogP ]:
0.35

[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C

[ Index of Refraction ]:
1.496

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
S22-S24/25-S36/37

[ RIDADR ]:
3276

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2928000090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2928000090

[ Summary ]:
2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

Articles

Carboxymethylcellulose-tetrahydrocurcumin conjugates for colon-specific delivery of a novel anti-cancer agent, 4-amino tetrahydrocurcumin.

Eur. J. Pharm. Biopharm. 88(2) , 351-60, (2014)

Several curcumin derivatives are now becoming increasingly of interest because of their bioactive attributes, especially their action as antioxidants and anti-carcinogenic activities. Tetrahydrocurcum...

COMU-Safer and More Efficient Peptide Coupling Reagent. Junkers M.
COMU-Safer and More Efficient Peptide Coupling Reagent.

Aldrich Chemfiles 10(1) , (2010)

Route to three-dimensional fragments using diversity-oriented synthesis.

Proc. Natl. Acad. Sci. U. S. A. 108(17) , 6799-804, (2011)

Fragment-based drug discovery (FBDD) has proven to be an effective means of producing high-quality chemical ligands as starting points for drug-discovery pursuits. The increasing number of clinical ca...