2-Nitrobenzenesulfonamide

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Names

[ CAS No. ]:
5455-59-4

[ Name ]:
2-Nitrobenzenesulfonamide

[Synonym ]:
2-Nitrobenzenesulfonamide
nitrobenzenesulfonamide
2-Nitro-benzenesulfonamide
Benzenesulfonamide, 2-nitro-
2-Sulphamoylnitrobenzene
2-Nitrobenzenesulphonamide
o-nitrobenzenesulfonamide
MFCD00009807
O-Nitrobenzenesulfonylamide
nitrophenylsulphonamide
1-(2-Methoxyphenyl)piperazine hydrochloride

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
418.8±47.0 °C at 760 mmHg

[ Melting Point ]:
189-194 °C

[ Molecular Formula ]:
C6H6N2O4S

[ Molecular Weight ]:
202.19

[ Flash Point ]:
207.1±29.3 °C

[ Exact Mass ]:
202.004822

[ PSA ]:
114.36000

[ LogP ]:
0.34

[ Vapour Pressure ]:
0.0±1.0 mmHg at 25°C

[ Index of Refraction ]:
1.611

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 ]:
S36/37/39-S26-S22-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2935009090

Synthetic Route

Precursor & DownStream

Precursor

  • o-Nitrophenylsulfonyl chloride
  • (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(1-((2-nitrophenyl)sulfonyl)-6-oxo-1,6-dihydro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
  • N-diazo-2-nitrobenzenesulfonamide

DownStream

  • 2-AMINO-5-BROMOBENZENESULPHONAMIDE
  • 2-Aminobenzenesulfonamide
  • tert-Butyl [(2-nitrophenyl)sulfonyl]carbamate
  • ethyl N-(2-nitrophenyl)sulfonylcarbamate
  • 2,5-Diaminobenzenesulfonamide
  • N-CARBOBENZOXY-2-NITROBENZENESULFONAMIDE
  • 2-nitro-N-pent-4-enylbenzenesulfonamide
  • Benzeneacetamide,2-nitro-
  • N-[(4-methoxyphenyl)methyl]-2-nitrobenzenesulfonamide
  • 1,1-dioxo-4H-1λ6,2,4-benzothiadiazin-3-one

Customs

[ HS Code ]: 2935009090

[ Summary ]:
2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0%

Articles

Total synthesis of polyamine toxin HO-416b and Agel-489 using a 2-nitrobenzenesulfonamide strategy.

Chem. Pharm. Bull. 48(10) , 1570-6, (2000)

Total synthesis of spider toxins HO-416b (1) and Agel-489 (2) was accomplished using the 2-nitrobenzenesulfonamide (Ns) group as both a protecting and activating group. In this strategy, the C-N bonds...


More Articles


Related Compounds

  • N-Cbz-2-nitrobenzenesulfonamide
  • N-Boc-2-nitrobenzenesulfonamide
  • N-ethyl-2-nitrobenzenesulfonamide
  • N-allyl 2-nitrobenzenesulfonamide
  • 5-Amino-2-nitrobenzenesulfonamide
  • N-butyl-2-nitrobenzenesulfonamide
  • 5-(2-phenylethyl)-2-Thiazolamine
  • 2-Amino-5-(2-chlorophenethyl)-1,3,4-thiadiazole
  • 1h-Indole-3-acetaldehyde,2-iodo-1-(phenylsulfonyl)-
  • [(E)-2-Aminoethenyl]dimethylamine
  • N-[(1,1-Dimethylethoxy)carbonyl]-L-alanylglycine 2-oxo-2-phenylethyl ester
  • Ethyl 2-[(5-bromo-3-methylpyridin-2-yl)oxy]propanoate
  • N-(2-(4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)quinazolin-5-yloxy)ethyl)-2-hydroxy-N-methylacetamide
  • Benzoic acid, 5-[(Z)-(2-amino-4-oxo-5(4H)-thiazolylidene)methyl]-2-hydroxy-
  • 6-Amino-10-chlorobenzo[c]quinolizinium
  • 7-Chloro-4-morpholin-4-ylquinazolin-8-ol