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Molecule
ID:57532
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₇N₃S
Molecular Mass
177.22628
Exact Mass
177.03606824
Charge
0
InChI
InChI=1S/C8H7N3S/c9-8-11-10-7(12-8)6-4-2-1-3-5-6/h1-5H,(H2,9,11)
InChIKey
UHZHEOAEJRHUBW-UHFFFAOYSA-N
Canonic Smiles
Nc1nnc(s1)c1ccccc1
Isomeric Smiles
s1c(nnc1N)c1ccccc1
Calculated Properties
JChem
Acid pKa
14.871872
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
1.6283793
LogD (pH = 7.4)
1.6283861
Log P
1.6283861
Molar Refractivity
60.6645
Polarizability
18.645304
Polar Surface Area
51.8
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
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
IUPAC name
•
Synonyms
•
IUPAC Traditional name
Registration numbers
•
PubChem SID
•
CAS Number
•
MDL Number
•
PubChem CID
Properties
•
Safety Information
•
Physical Property
•
Product Information
Related Proteins
Molecular Spectra
Molecule Details
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR13738
Life Chemicals
F1386-0081
Sigma Aldrich
438537
Enamine
EN300-13036
Alfa Aesar
H32826
Matrix Scientific
062708
Academic Data
PubChem
219408
Names and Identifiers
IUPAC name
5-phenyl-1,3,4-thiadiazol-2-amine
Synonyms
5-Phenyl-1,3,4-thiadiazol-2-amine
2-Amino-5-phenyl-1,3,4-thiadiazole
2-氨基-5-苯基-1,3,4-噻二唑
5-Phenyl-1,3,4-thiadiazol-2-amine
2-Amino-5-phenyl-1,3,4-thiadiazole
5-Phenyl-[1,3,4]thiadiazol-2-ylamine
2-氨基-5-苯基-1,3,4-硫杂二唑
IUPAC Traditional name
5-phenyl-1,3,4-thiadiazol-2-amine
Registration numbers
PubChem SID
24867459
162062295
CAS Number
2002-03-1
MDL Number
MFCD00205278
PubChem CID
219408
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Risk Statements
36/37/38
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Safety Statements
26
-
36
Source
26
-
37
Source
GHS Signal Word
Warning
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
German water hazard class
3
Source
European Hazard Symbols
Irritant (Xi)
Source
Physical Property
Partition Coefficient
3.039
Source
Melting Point
223-227 °C(lit.)
Source
218 - 220°C
Source
227-230°C
Source
Hydrophobicity(logP)
1.492
Source
Product Information
Purity
95+%
Source
96%
Source
95%
Source
97%
Source
Empirical Formula (Hill Notation)
C8H7N3S
Source
Molecule Details
Sigma Aldrich
438537
Packaging
1 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay