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Molecule
ID:75235
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₈N₂S
Molecular Mass
152.21682
Exact Mass
152.04081927
Charge
0
InChI
InChI=1S/C7H8N2S/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,8H2,(H2,9,10)
InChIKey
LZJVSPPXXGXGQL-UHFFFAOYSA-N
Canonic Smiles
Nc1ccc(cc1)C(=S)N
Isomeric Smiles
Nc1ccc(cc1)C(=S)N
Calculated Properties
JChem
Acid pKa
13.420398
H Acceptors
1
H Donor
2
LogD (pH = 5.5)
0.8714797
LogD (pH = 7.4)
0.88465947
Log P
0.88482976
Molar Refractivity
47.8277
Polarizability
17.688194
Polar Surface Area
52.04
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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Related Proteins
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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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General Information
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IUPAC name
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Synonyms
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IUPAC Traditional name
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CAS Number
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MDL Number
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PubChem SID
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PubChem CID
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Product Information
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Molecular Spectra
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Sigma Aldrich
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From Data Sources
Bioactivity
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Data Source
Commercial Catalog
Apollo Scientific
OR11119
Sigma Aldrich
724904
Enamine
EN300-40101
A&J Pharmtech
AJA-O38639
Academic Data
PubChem
2756559
Names and Identifiers
IUPAC name
4-aminobenzene-1-carbothioamide
Synonyms
4-Aminothiobenzamide
4-Aminobenzothioamide
4-Aminothiobenzamide
4-Aminobenzenecarbothioamide
4-aminobenzenecarbothioamide
IUPAC Traditional name
benzamide, p-aminothio-
Registration numbers
CAS Number
4714-67-4
4114-67-4
MDL Number
MFCD00040927
PubChem SID
162040153
PubChem CID
2756559
Properties
Safety Information
Storage Warning
Irritant
Source
GHS Signal Word
Warning
Source
Safety Statements
26
-
36/37/39
Source
MSDS Link
Download link
Source
German water hazard class
3
Source
Risk Statements
22
-
36
-
43
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
GHS Precautionary statements
P280
-
P305+P351+P338
Source
GHS Hazard statements
H302
-
H317
-
H319
Source
European Hazard Symbols
Harmful (Xn)
Source
Physical Property
Melting Point
185-190 °C
Source
189 - 191°C
Source
Hydrophobicity(logP)
0.428
Source
Product Information
Purity
97%
Source
95%
Source
98%
Source
Empirical Formula (Hill Notation)
C7H8N2S
Source
Molecule Details
Sigma Aldrich
724904
Packaging
1 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay