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2-NITRO-5-(PHENYLACETYLAMINO)-BENZOIC ACID

Names

[ CAS No. ]:
52033-70-2

[ Name ]:
2-NITRO-5-(PHENYLACETYLAMINO)-BENZOIC ACID

[Synonym ]:
6-Nitro-3-(phenylacetamido)benzoic acid
6-Nitro-3-phenylacetamidobenzoesaeure
2-nitro-5-(2-phenylacetylamino)benzoic acid
NIPAB
2-Nitro-5-[(phenylacetyl)amino]benzoic acid

Chemical & Physical Properties

[ Density]:
1.446g/cm3

[ Boiling Point ]:
599.6ºC at 760 mmHg

[ Molecular Formula ]:
C15H12N2O5

[ Molecular Weight ]:
300.26600

[ Flash Point ]:
316.4ºC

[ Exact Mass ]:
300.07500

[ PSA ]:
112.22000

[ LogP ]:
3.07040

[ Index of Refraction ]:
1.68

[ Storage condition ]:
2-8°C

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H315-H318-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

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

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R37/38

[ Safety Phrases ]:
26-36/37/39

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2924299090

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2924299090

[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Improving the diastereoselectivity of penicillin G acylase for ampicillin synthesis from racemic substrates.

Protein Eng. Des. Sel. 25(3) , 135-44, (2012)

Semi-synthetic β-lactam antibiotics are synthesized enzymatically with the use of penicillin G acylase (PGA). Currently, PGA only exhibits weak diastereoselectivity with respect to the alpha amino gro...

Preparation and general properties of crystalline penicillin acylase from Escherichia coli ATCC 11 105.

Hoppe. Seylers. Z. Physiol. Chem. 354 , 45, (1974)

New active site oriented glyoxyl-agarose derivatives of Escherichia coli penicillin G acylase.

BMC Biotechnol. 7 , 54, (2007)

Immobilized Penicillin G Acylase (PGA) derivatives are biocatalysts that are industrially used for the hydrolysis of Penicillin G by fermentation and for the kinetically controlled synthesis of semi-s...


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Related Compounds