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Molecule
ID:74365
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₁Cl₂N₅
Molecular Mass
248.11244
Exact Mass
247.03915074
Charge
0
InChI
InChI=1S/C8H10ClN5.ClH/c9-5-2-1-3-6(4-5)13-8(12)14-7(10)11;/h1-4H,(H6,10,11,12,13,14);1H
InChIKey
FOWAIJYHRWFTHR-UHFFFAOYSA-N
Canonic Smiles
NC(=N)NC(=N)Nc1cccc(c1)Cl.Cl
Isomeric Smiles
N(c1cc(ccc1)Cl)C(=N)NC(=N)N.Cl
Calculated Properties
JChem
H Acceptors
5
H Donor
5
LogD (pH = 5.5)
-3.2587626
LogD (pH = 7.4)
-1.6481558
Log P
1.3301078
Molar Refractivity
77.7112
Polarizability
20.776552
Polar Surface Area
97.78
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 Traditional name
•
Synonyms
•
IUPAC name
Registration numbers
•
MDL Number
•
CAS Number
•
PubChem SID
•
PubChem CID
Properties
•
Safety Information
•
Product Information
•
Physical Property
•
Pharmacology Properties
Related Proteins
Molecular Spectra
Molecule Details
•
MP Biomedicals
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR0928
MP Biomedicals
02159751
Sigma Aldrich
C144
572225
Alfa Aesar
B20355
Academic Data
PubChem
2730228
Names and Identifiers
IUPAC Traditional name
m-chlorophenylbiguanide hydrochloride
Synonyms
{[(3-Chloroanilino)(imino)methyl]amino}methanimidamide hydrochloride
1-(3-Chlorophenyl)biguanide hydrochloride
N-(3-Chlorophenyl)imidodicarbonimidic diamide hydrochloride
1-(m-Chlorophenyl)biguanide hydrochloride
1-(3-Chlorophenyl)biguanide hydrochloride
m-CPBG hydrochloride
1-(3-氯苯基)双胍 盐酸盐
IUPAC name
1-carbamimidamido-N-(3-chlorophenyl)methanimidamide hydrochloride
Registration numbers
MDL Number
MFCD00053019
CAS Number
2113-05-5
PubChem SID
24874788
24278089
162039284
PubChem CID
2730228
Properties
Safety Information
Storage Warning
Irritant
Source
Hygroscopic
Source
Storage Condition
Room Temperature (15-30°C)
Source
RTECS
DU1780000
Source
MSDS Link
Download link
Source
Download link
Source
GHS Signal Word
Warning
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
German water hazard class
3
Source
Risk Statements
36/37/38
Source
Safety Statements
26
-
36
Source
26
-
37
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
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
TSCA Listed
否
Source
Product Information
Certificate of Analysis
Download link
Source
Purity
97%
Source
Linear Formula
ClC6H4NHC(NH)NHC(NH)NH2 · HCl
Source
Physical Property
Melting Point
190-194 °C(lit.)
Source
191-194°C
Source
Solubility
H2O: soluble
Source
Apperance
white solid
Source
Pharmacology Properties
Gene Information
human ... HTR3A(3359), HTR3B(9177), HTR3C(170572), HTR3D(200909), HTR3E(285242)
Source
Molecule Details
MP Biomedicals
02159751
Hydrochloride
Specific agonist for 5-HT
3
receptor.
Sigma Aldrich
C144
Biochem/physiol Actions
Very potent 5-HT3 serotonin receptor agonist.
References
PubChem Literature
From Data Sources
•
Sepulveda, et al.,
Br. J. Pharmacol.
, 104 : 536 (1991).
Bioactivity
PubChem BioAssay