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96-96-8 molecular structure
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4-methoxy-2-nitroaniline

ChemBase ID: 69019
Molecular Formular: C7H8N2O3
Molecular Mass: 168.15002
Monoisotopic Mass: 168.05349213
SMILES and InChIs

SMILES:
Nc1c(cc(cc1)OC)[N+](=O)[O-]
Canonical SMILES:
COc1ccc(c(c1)[N+](=O)[O-])N
InChI:
InChI=1S/C7H8N2O3/c1-12-5-2-3-6(8)7(4-5)9(10)11/h2-4H,8H2,1H3
InChIKey:
QFMJFXFXQAFGBO-UHFFFAOYSA-N

Cite this record

CBID:69019 http://www.chembase.cn/molecule-69019.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
4-methoxy-2-nitroaniline
IUPAC Traditional name
fast bordeaux GP
Synonyms
4-AMINO-3-NITROANISOLE
4-Amino-3-nitroanisole
4-Methoxy-2-nitroaniline
2-Nitro-p-anisidine
4-Methoxy-2-nitroaniline
4-Methoxy-2-nitrobenzenediazonium chloride hemi(zinc chloride) salt
Fast Bordeaux GP salt
Symulon Bordeaux GP Base
Tulabase Fast Bordeaux GP
o-Nitro-p-anisidine
p-Methoxy-o-nitroaniline
2-Nitro-p-anisidine
1-Amino-2-nitro-4-methoxybenzene
2-Nitro-4-methoxyaniline
2-Nitro-4-methoxybenzenamine
3-Nitro-4-aminoanisole
4-Amino-1-methoxy-3-nitrobenzene
4-Methoxy-2-nitroaniline
4-Methoxy-2-nitrobenzenamine
4-Methoxy-2-nitrohbenzenamine
4-Methoxy-2-nitrophenylamine
4-Methoxy-o-nitroaniline
Acco Fast Bordeaux GP salt
Amarthol Fast Bordeaux GP Base
Amarthol Fast Bordeaux GP Salt
Atul Fast Bordeaux GP Base
Azobase NAS
Azoene Fast Bordeaux GP Base
Azoene Fast Bordeaux GP Salt
Azofix Bordeaux GP
Azogene Fast Bordeaux G
Bordeaux Base Ciba IV
Bordeaux Base Irga IV
Bordeaux Base NGP
Bordeaux GP Base
Bordeaux GP Salt
Bordeaux GPS Salt
Bordeaux Salt Ciba IV
Bordeaux Salt NGP
Brentamine Fast Bordeaux GP Base
Daito Bordeaux Base GP
Daito Bordeaux Salt GP
Devol Bordeaux B
Devol Bordeaux GP Salt
Diabase Bordeaux GP
Diasalt Bordeaux GP
Durgasol Bordeaux GP Salt
Fast Bordeaux 3NA Base
Fast Bordeaux Base GP
Fast Bordeaux Base J
Fast Bordeaux GDN
Fast Bordeaux GDN base
Fast Bordeaux GP
Fast Bordeaux GP Base
Fast Bordeaux GP-T Base
Fast Bordeaux Salt GP
Fast Bordeaux Salt GPN
Fast Bordeaux Salt J
Hansol Bordeaux GP Salt
Hiltonil Fast Bordeaux GP Base
Hiltosal Fast Bordeaux GP Salt
Hindasol Bordeaux GP Salt
Kako Bordeaux GP Base
Kako Bordeaux GP Salt
Kayaku Fast Bordeaux GP Base
Kayaku Fast Bordeaux Salt GP
Lake Maroon B base
Mitsui Bordeaux GP Base
Mitsui Bordeaux GP Salt
NSC 5509
Naphthanil Bordeaux GP Base
Naphthanil Diazo Bordeaux GP
Naphthosol Fast Bordeaux GP Salt
Naphtoelan Fast Bordeaux GP Base
Naphtoelan Fast Bordeaux GP Salt
Natasol Bordeaux GP Salt
Pharmasol Bordeaux GP
Pharmazoid Bordeaux GP
Sanyo Fast Bordeaux GP Base
Sanyo Fast Bordeaux Salt GP
Shinnippon Fast Bordeaux GP Base
Sugai Fast Bordeaux GP Base
2-硝基对茴香胺
4-氨基-3-硝基苯甲醚
4-甲氧基-2-硝基苯胺
CAS Number
96-96-8
EC Number
202-547-2
MDL Number
MFCD00007152
MFCD00135644
Beilstein Number
880318
PubChem SID
24896683
162034748
24886441
PubChem CID
66793
Color Index Number
37135

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 16.51667  H Acceptors
H Donor LogD (pH = 5.5) 1.5766202 
LogD (pH = 7.4) 1.5766326  Log P 1.5766327 
Molar Refractivity 43.5421 cm3 Polarizability 15.916087 Å3
Polar Surface Area 78.39 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
Dichloromethane expand Show data source
Ethyl Acetate expand Show data source
Methanol expand Show data source
Apperance
Orange Solid expand Show data source
Melting Point
123-125 °C expand Show data source
123-126 °C(lit.) expand Show data source
123-126°C expand Show data source
126-128°C expand Show data source
Storage Warning
IRRITANT expand Show data source
Very Toxic expand Show data source
RTECS
BY4415000 expand Show data source
European Hazard Symbols
Highly toxic Highly toxic (T+) expand Show data source
UN Number
2811 expand Show data source
UN2811 expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
2 expand Show data source
3 expand Show data source
Hazard Class
6.1 expand Show data source
Packing Group
2 expand Show data source
II expand Show data source
Risk Statements
26/27/28-33-52/53 expand Show data source
R:26/27/28-33-52/53 expand Show data source
Safety Statements
28-36/37-45-61 expand Show data source
S:28-45-61-36/37 expand Show data source
TSCA Listed
false expand Show data source
expand Show data source
GHS Pictograms
GHS06 expand Show data source
GHS08 expand Show data source
GHS Signal Word
Danger expand Show data source
GHS Hazard statements
H300-H310-H330-H373-H402-H412 expand Show data source
H300-H310-H330-H373-H412 expand Show data source
GHS Precautionary statements
P260-P264-P273-P280-P284-P302 + P350 expand Show data source
P260-P301+P310-P304+P340-P320-P330-P361-P405-P501A expand Show data source
Personal Protective Equipment
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges expand Show data source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
RID/ADR
UN 2811 6.1/PG 2 expand Show data source
Storage Temperature
-20°C expand Show data source
Purity
≥90% (T) expand Show data source
95+% expand Show data source
97% expand Show data source
98% expand Show data source
99% expand Show data source
Grade
technical expand Show data source
Certificate of Analysis
Download expand Show data source
Download expand Show data source
Linear Formula
CH3OC6H3(NO2)NH2 expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals Sigma Aldrich Sigma Aldrich TRC TRC
MP Biomedicals - 05202046 external link
MP Biomedicals Rare Chemical collection
Sigma Aldrich - M17403 external link
Packaging
100, 500 g in glass bottle
Toronto Research Chemicals - N491800 external link
Toxic to some wild and domestic birds and mice. Molluscicidal activity

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • De Abreu, F. et al.; Bioorg. Med. Chem. 9, 659 (2001)
  • • Schafer, E.W. et al.; Arch. Environ. Con. Tox. 14, 111 (2001)
  • • Schafer, E.W. et al.; Arch. Environ. Con. Tox. 12, 355 (1983)
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PATENTS

PATENTS

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INTERNET

INTERNET

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