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Molecule
ID:61702
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₅N₃O₂
Molecular Mass
163.1335
Exact Mass
163.03817642
Charge
0
InChI
InChI=1S/C7H5N3O2/c8-4-5-1-2-6(9)7(3-5)10(11)12/h1-3H,9H2
InChIKey
JAHADAZIDZMHOP-UHFFFAOYSA-N
Canonic Smiles
N#Cc1ccc(c(c1)[N+](=O)[O-])N
Isomeric Smiles
C(#N)c1cc(c(cc1)N)[N+](=O)[O-]
Calculated Properties
JChem
Acid pKa
12.863087
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
1.5904002
LogD (pH = 7.4)
1.5904002
Log P
1.5904002
Molar Refractivity
42.8005
Polarizability
15.223141
Polar Surface Area
92.95
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
No Data Available
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
Synonyms
•
IUPAC name
•
IUPAC Traditional name
Registration numbers
Properties
•
Product Information
•
Safety Information
•
Physical Property
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
•
TRC
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR01561
Matrix Scientific
066947
Sigma Aldrich
324698
08857
TRC
A618398
Chemik
CHB27881
Enamine
EN300-19048
Bide Pharmatech
BD10391
Alfa Aesar
B23463
Academic Data
PubChem
595901
Names and Identifiers
Synonyms
4-Amino-3-nitrobenzonitrile
4-Cyano-2-nitroaniline
4-Amino-3-nitrobenzonitrile
4-氨基-3-硝基苯甲腈
3-Nitro-4-aminobenzonitrile
2-Nitro-4-cyanoaniline
4-Amino-3-nitrobenzonitrile
IUPAC name
4-amino-3-nitrobenzonitrile
IUPAC Traditional name
4-amino-3-nitrobenzonitrile
Registration numbers
CAS Number
6393-40-4
PubChem SID
24846228
24859461
162027443
Beilstein Number
778939
MDL Number
MFCD00013373
PubChem CID
595901
Molecule Details
Sigma Aldrich
324698
Packaging
5 g in glass bottle
TRC
A618398
Gamma irradiations effect on release of 4-amino-3-nitrobenzonitrile from polyanhydride matrixes.
References
PubChem Literature
From Data Sources
•
Leong, K., et al.: J. Biomaterials Res., 20, 51 (1986)
•
865 (1986)
•
Domb, A., et al.: Pharma. Res., 11(1986)
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
PubChem SID
•
Beilstein Number
•
MDL Number
•
PubChem CID
Properties
Product Information
Purity
98%
Source
≥97.0% (GC)
Source
95%
Source
Linear Formula
H2NC6H3(NO2)CN
Source
Grade
purum
Source
Certificate of Analysis
Download link
Source
Safety Information
Storage Warning
IRRITANT
Source
Toxic/Harmful/Irritant/Light Sensitive/Keep Cold
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Warning
Source
Irritant (Xi)
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
H315
-
H319
-
H335
Source
H331
-
H302
-
H312
-
H315
-
H319
-
H335
Source
dust mask type N95 (US), Eyeshields, Gloves
Source
36/37/38
Source
20/21/22
-
36/37/38
Source
3
Source
26
-
36
Source
9
-
26
-
36/37
Source
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
UN3439
Source
III
Source
6.1
Source
Physical Property
Melting Point
158-161°C
Source
159-162°C
Source
159-162 °C(lit.)
Source
159-162 °C
Source
161 - 163°C
Source
159-161°C
Source
Apperance
Yellow Powder
Source
1.491
Source
Source
Harmful (X)
Source
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Source
GHS Signal Word
European Hazard Symbols
GHS Precautionary statements
GHS Hazard statements
Personal Protective Equipment
Risk Statements
German water hazard class
Safety Statements
GHS Pictograms
UN Number
Packing Group
Hazard Class
Hydrophobicity(logP)