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Molecule
ID:11779
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₆ClN
Molecular Mass
151.59294
Exact Mass
151.01887688
Charge
0
InChI
InChI=1S/C8H6ClN/c9-7-2-1-3-8-6(7)4-5-10-8/h1-5,10H
InChIKey
SVLZRCRXNHITBY-UHFFFAOYSA-N
Canonic Smiles
Clc1cccc2c1cc[nH]2
Isomeric Smiles
c1(Cl)c2c(ccc1)[nH]cc2
Calculated Properties
JChem
Acid pKa
16.102888
H Acceptors
0
H Donor
1
LogD (pH = 5.5)
2.6760526
LogD (pH = 7.4)
2.6760526
Log P
2.6760526
Molar Refractivity
41.9493
Polarizability
17.424847
Polar Surface Area
15.79
Rotatable Bonds
0
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
•
IUPAC Traditional name
•
IUPAC name
•
Synonyms
Registration numbers
Properties
•
Safety Information
•
Physical Property
•
Product Information
Related Proteins
Molecular Spectra
Molecule Details
•
MP Biomedicals
•
Sigma Aldrich
•
TRC
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
ChemBridge
3020086
Apollo Scientific
OR6700T
MP Biomedicals
02199466
Matrix Scientific
008756
InterBioScreen
BB_SC-10939
Sigma Aldrich
246220
24912
TRC
C367000
Enamine
EN300-98385
Bide Pharmatech
BD10950
A&J Pharmtech
AJA-O38275
Academic Data
PubChem
91345
Names and Identifiers
IUPAC Traditional name
4-chloro-1H-indole
IUPAC name
4-chloro-1H-indole
Synonyms
4-Chloro-1H-indole
4-Chloroindole
4-Chloroindole
4-氯吲哚
4-Chloro-1H-indole
NSC 88141
Registration numbers
CAS Number
25235-85-2
136669-25-5
MDL Number
MFCD00005665
PubChem CID
91345
PubChem SID
160975086
24854796
EC Number
246-747-8
Beilstein Number
114880
Molecule Details
MP Biomedicals
02199466
Purity: 99%
Light yellow liquid.
Sigma Aldrich
246220
Packaging
1 g in glass bottle
24912
Caution
may discolor on storage
TRC
C367000
Indole derivative. Inhibitor
References
PubChem Literature
From Data Sources
•
Jadhav, A. L., et al.: Drug Dev. Res., 23, 83 (1991)
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
PubChem CID
•
PubChem SID
•
EC Number
•
Beilstein Number
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
IRRITANT
Source
Irritant
Source
Irritant (Xi)
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
3
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
P261
-
P305+P351+P338
Source
26
-
36
Source
36/37/38
Source
H315
-
H319
-
H335
Source
Warning
Source
2-8°C
Source
Physical Property
129-130°C/4mm
Source
129-130 °C/4 mmHg(lit.)
Source
95-100°C/0.5 mm Hg
Source
1.259
Source
1.259 g/mL at 25 °C(lit.)
Source
1.6280
Source
n20/D 1.628(lit.)
Product Information
99%
Source
98%
Source
≥97.0% (GC)
Source
95%
Source
Download link
Source
Download link
Source
Source
Source
Source
235.4 °F
Source
113 °C
Source
clear yellow liquid (clear)
Source
Light-Yellow Liquid
Source
Methanol
Source
Chloroform
Source
3.013
Source
C8H6ClN
Source
purum
Source
Storage Warning
European Hazard Symbols
Personal Protective Equipment
German water hazard class
GHS Pictograms
GHS Precautionary statements
Safety Statements
Risk Statements
GHS Hazard statements
GHS Signal Word
Storage Temperature
Boiling Point
Density
Refractive Index
Purity
Certificate of Analysis
Flash Point
Apperance
Solubility
Hydrophobicity(logP)
Empirical Formula (Hill Notation)
Grade