Molfinder
Home
Support
About Us
Data Source
Statistics
Blogs
Molecule
ID:70127
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₅NO₄
Molecular Mass
167.1189
Exact Mass
167.02185765
Charge
0
InChI
InChI=1S/C7H5NO4/c9-4-5-1-2-6(8(11)12)7(10)3-5/h1-4,10H
InChIKey
AUBBVPIQUDFRQI-UHFFFAOYSA-N
Canonic Smiles
O=Cc1ccc(c(c1)O)[N+](=O)[O-]
Isomeric Smiles
C(=O)c1cc(c(cc1)[N+](=O)[O-])O
Calculated Properties
JChem
Acid pKa
6.0821686
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
1.2223202
LogD (pH = 7.4)
0.064630255
Log P
1.322167
Molar Refractivity
40.9434
Polarizability
14.816353
Polar Surface Area
80.44
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
Loading...
Names and Identifiers
Loading...
Registration numbers
Loading...
Properties
Loading...
Related Proteins
No Data Available
Click here to submit data
Molecular Spectra
No Data Available
Click here to submit data
Molecule Details
Loading...
References
Loading...
Bioactivity
Loading...
Quote
Download
Navigation
General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Academic Data
•
Commercial Catalog
Names and Identifiers
•
IUPAC name
•
IUPAC Traditional name
•
Synonyms
Registration numbers
Properties
•
Safety Information
•
Product Information
•
Physical Property
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Academic Data
PubChem
69712
Commercial Catalog
Sigma Aldrich
156167
55969
Enamine
EN300-61110
Matrix Scientific
075653
Bide Pharmatech
BD10394
A&J Pharmtech
AJA-O38397
Names and Identifiers
IUPAC name
3-hydroxy-4-nitrobenzaldehyde
IUPAC Traditional name
3-hydroxy-4-nitrobenzaldehyde
Synonyms
3-Hydroxy-4-nitrobenzaldehyde
3-Hydroxy-4-nitrobenzaldehyde
3-羟基-4-硝基苯甲醛
Registration numbers
PubChem CID
69712
MDL Number
MFCD00007109
PubChem SID
162035852
24879634
24849596
Beilstein Number
2556882
EC Number
211-879-7
CAS Number
704-13-2
Properties
Safety Information
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Risk Statements
36/37/38
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
Safety Statements
26
-
36
Source
GHS Signal Word
Warning
Source
German water hazard class
3
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Pictograms
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
Source
Product Information
Purity
95+%
Source
97%
Source
≥98.0% (GC)
Source
95%
Source
98%
Source
Linear Formula
HOC6H3(NO2)CHO
Source
Grade
purum
Source
Physical Property
Melting Point
127-131 °C(lit.)
Source
127-131 °C
Source
132 - 134°C
Source
Apperance
yellow
Source
Hydrophobicity(logP)
1.501
Source
Molecule Details
Sigma Aldrich
156167
Application
Aldehyde component in a study of an enantioselective thioester aldol reaction catalyzed by copper(II) triflate in the presence of a chiral bisoxazoline ligand.1
Packaging
1 g in glass bottle
10 g in poly bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
PubChem CID
•
MDL Number
•
PubChem SID
•
Beilstein Number
•
EC Number
•
CAS Number