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Molecule
ID:67659
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₆OS
Molecular Mass
162.20834
Exact Mass
162.01393581
Charge
0
InChI
InChI=1S/C9H6OS/c10-5-7-6-11-9-4-2-1-3-8(7)9/h1-6H
InChIKey
WDJLPQCBTBZTRH-UHFFFAOYSA-N
Canonic Smiles
O=Cc1csc2c1cccc2
Isomeric Smiles
c12c(c(cs1)C=O)cccc2
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.561773
LogD (pH = 7.4)
2.561773
Log P
2.561773
Molar Refractivity
45.9821
Polarizability
18.412346
Polar Surface Area
17.07
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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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
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Molecule Details
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References
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Bioactivity
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR23174
Maybridge
CC12304
Matrix Scientific
073096
Sigma Aldrich
494968
Enamine
EN300-24744
Bide Pharmatech
BD7340
Academic Data
PubChem
227328
Names and Identifiers
Synonyms
Benzo[b]thiophene-3-carboxaldehyde
3-Formylbenzo[b]thiophene
Benzo[b]thiophene-3-carboxaldehyde 95%
苯并噻酚-3-甲醛
Benzo[b]thiophene-3-carboxaldehyde
3-甲醛苯并噻吩
Thianaphthene-3-carboxaldehyde
1-benzothiophene-3-carbaldehyde
Benzo[b]thiophene-3-carbaldehyde
IUPAC name
1-benzothiophene-3-carbaldehyde
IUPAC Traditional name
1-benzothiophene-3-carbaldehyde
Registration numbers
CAS Number
5381-20-4
MDL Number
MFCD00052376
PubChem SID
24872938
162033394
PubChem CID
227328
Molecule Details
Sigma Aldrich
494968
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Irritant
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
Product Information
95+%
Source
97%
Source
95%
Source
C9H6OS
Source
Physical Property
166°C/20mm
Source
166 °C/20 mmHg(lit.)
Source
>110°C
Source
>113 °C
Source
>235.4 °F
Source
53-57°C
Source
53-57 °C(lit.)
Source
53 - 57°C
Source
2.7
Source
Personal Protective Equipment
German water hazard class
Purity
Empirical Formula (Hill Notation)
Boiling Point
Flash Point
Melting Point
Hydrophobicity(logP)