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Molecule
ID:15614
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₇NO
Molecular Mass
145.15798
Exact Mass
145.05276385
Charge
0
InChI
InChI=1S/C9H7NO/c11-6-8-5-7-3-1-2-4-9(7)10-8/h1-6,10H
InChIKey
SBNOTUDDIXOFSN-UHFFFAOYSA-N
Canonic Smiles
O=Cc1cc2c([nH]1)cccc2
Isomeric Smiles
c1ccc2c(c1)[nH]c(c2)C=O
Calculated Properties
JChem
Acid pKa
12.765318
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
1.7045113
LogD (pH = 7.4)
1.7045096
Log P
1.7045113
Molar Refractivity
43.606
Polarizability
17.474945
Polar Surface Area
32.86
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
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Commercial Catalog
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC name
•
IUPAC Traditional name
Registration numbers
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MDL Number
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CAS Number
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PubChem CID
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PubChem SID
Properties
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Safety Information
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Physical Property
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR5662
Key Organics
CF-0774
Matrix Scientific
016204
Sigma Aldrich
687782
ChemBridge
4130840
Alfa Aesar
H54638
A&J Pharmtech
AJA-O34341
Academic Data
PubChem
96389
Names and Identifiers
Synonyms
1H-Indole-2-carboxaldehyde
1H-Indole-2-carbaldehyde
2-Formyl-1H-indole
吲哚-2-甲醛
Indole-2-carboxaldehyde
IUPAC name
1H-indole-2-carbaldehyde
IUPAC Traditional name
1H-indole-2-carbaldehyde
Registration numbers
MDL Number
MFCD03001425
CAS Number
19005-93-7
PubChem CID
96389
PubChem SID
160978921
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT
Source
Irritant/Light Sensitive/Keep Cold/Store under Argon
Source
Air Sensitive
Source
GHS Signal Word
Warning
Source
GHS Hazard statements
H319
Source
European Hazard Symbols
Irritant (Xi)
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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
Risk Statements
36
Source
Safety Statements
26
-
36
Source
26
-
60
Source
GHS Precautionary statements
P305+P351+P338
Source
P280
-
P264
-
P305+P351+P338
-
P337+P313
Source
German water hazard class
3
Source
Physical Property
Melting Point
138-142 °C
Source
138-142°C
Source
141 - 142 °C
Source
138-142 °C
Source
138-142°C
Source
Product Information
Purity
>95%
Source
97%
Source
98%
Source
Empirical Formula (Hill Notation)
C9H7NO
Source
Molecule Details
Sigma Aldrich
687782
Application
Useful starter in indole and natural product chemistry1,2
Packaging
1 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay