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Molecule
ID:108263
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₄N₂
Molecular Mass
104.10936
Exact Mass
104.03744814
Charge
0
InChI
InChI=1S/C6H4N2/c7-5-6-3-1-2-4-8-6/h1-4H
InChIKey
FFNVQNRYTPFDDP-UHFFFAOYSA-N
Canonic Smiles
N#Cc1ccccn1
Isomeric Smiles
N#Cc1ccccn1
Calculated Properties
JChem
LogD (pH = 7.4)
1.00
LogD (pH = 5.5)
1.00
Log P
1.00
Rotatable Bonds
0
H Donor
0
H Acceptors
2
Lipinski's Rule of Five
true
Acid pKa
0.98
Polar Surface Area
36.68
Polarizability
10.22
Molar Refractivity
29.25
LOG S
-0.66
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
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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
•
IUPAC Traditional name
•
Synonyms
Registration numbers
Properties
•
Safety Information
•
Product Information
•
Physical Property
Related Proteins
Molecular Spectra
Molecule Details
•
MP Biomedicals
•
Sigma Aldrich
•
TRC
•
ChEBI
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
05206715
InterBioScreen
BB_SC-8696
Sigma Aldrich
C94602
28570
TRC
C982170
Chemik
CHH00191
Bide Pharmatech
BD40078
Alfa Aesar
A12900
A&J Pharmtech
AJA-O511
Academic Data
PubChem
7522
ChEBI
CHEBI:27837
Names and Identifiers
IUPAC name
pyridine-2-carbonitrile
IUPAC Traditional name
2-cyanopyridine
Synonyms
2-CYANOPYRIDINE
picolinonitrile
Picolinonitrile
2-氰基吡啶
2-Pyridinecarbonitrile
2-Cyanopyridine
2-吡啶甲腈
2-Azabenzonitrile
2-Pyridyl Cyanide
NSC 59697
2-Pyridinenitrile
α-Cyanopyridine
Picolinic Acid Nitrile
2-Pyridylnitrile
Pyridine-2-carbonitrile
2-Pyridinecarbonitrile
2-氰基吡啶
2-Cyanopyridine
Picolinic acid nitrile
Picolinonitrile
2-Pyridinecarboxylic acid, nitrile
2-Cyanopyridine
2-cyanopyridine
pyridine-2-carbonitrile
2-Pyridyl nitrile
2-Pyridinecarbonitrile
Registration numbers
EC Number
202-880-3
CAS Number
100-70-9
PubChem SID
162094026
24893000
26744159
PubChem CID
7522
Beilstein Number
107710
MDL Number
MFCD00006218
CHEMBL
CHEMBL3185861
BRENDA Ligand Database
121823
1991
154958
2883
2736
MetaboLights Database
MTBLS804
MTBLS2878
MTBLS1693
BKMS React Database
1991
154958
2736
2883
121823
CHEBI ID
CHEBI:1048
CHEBI:19518
CHEBI:27837
BRENDA Database
3.5.5.5
4.2.1.84
4.8.1.4
4.2.1.66
3.5.5.7
3.5.5.1
4.8.1.2
SureChEMBL Database
SCHEMBL129466
SABIO-RK Database
6765
Patent number
EP1422221
EP1238977
WO2005012306
WO2006091592
WO2005035507
WO2005095401
ACToR Database
100-70-9
29386-66-1
PubMed Citation Links
16909267
23202484
CompTox Database
DTXSID9021843
NMRShiftDB Database
20027634
KEGG ID
C02221
Reaxys Registry
107710
Molecule Details
MP Biomedicals
05206715
MP Biomedicals Rare Chemical collection
Sigma Aldrich
C94602
Packaging
5, 100, 500 g in glass bottle
28570
Caution
may discolor to light-brown on storage
Other Notes
Precursor of the appropriate amidate for the modification of proteins via amidation1
TRC
C982170
2-Cyanopyridine is a cyano substituted pyridine. 2-Cyanopyridine is a related compound of nicotine and is a component of tobacco smoke condensate.
ChEBI
CHEBI:27837
A cyanopyridine carrying the cyano group at position 2.
References
PubChem Literature
From Data Sources
•
Matsushima, S. et al.: Beit. Tabakforsch. Int., 10, 31 (1979)
•
French, R.C. et al.: Physiol. Plant Pathol., 19, 201 (1979)
Bioactivity
PubChem BioAssay
Registration numbers
•
EC Number
•
CAS Number
•
PubChem SID
•
PubChem CID
•
Beilstein Number
•
MDL Number
•
CHEMBL
•
BRENDA Ligand Database
•
MetaboLights Database
•
BKMS React Database
•
CHEBI ID
•
BRENDA Database
•
SureChEMBL Database
•
SABIO-RK Database
•
Patent number
•
ACToR Database
•
PubMed Citation Links
•
CompTox Database
•
NMRShiftDB Database
•
KEGG ID
•
Reaxys Registry
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Safety Statements
26
Source
26
-
36
Source
Warning
Source
dust mask type N95 (US), Eyeshields, Gloves
Source
P261
-
P305+P351+P338
Source
P280F-
P305+P351+P338
Source
Harmful (Xn)
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
H302
-
H315
-
H319
-
H335
Source
H302
-
H319
Source
22
-
36/37/38
Source
22
-
36
Source
3
Source
2-8°C
Source
是
Source
Product Information
Download link
Source
Download link
Source
99%
Source
≥98.0% (GC)
Source
98%
Source
C6H4N2
Source
Physical Property
24-27 °C(lit.)
Source
24-27 °C
Source
26-28°C
Source
89 °C
Source
192.2 °F
Source
89°C(192°F)
Source
212-215 °C(lit.)
Source
Source
Harmful (X)
Source
Source
Grade
purum
Source
212-214°C
Source
Refractive Index
n20/D 1.529(lit.)
Source
1.5290
Source
Density
1.081 g/mL at 25 °C(lit.)
Source
1.081
Source
GHS Signal Word
Personal Protective Equipment
GHS Precautionary statements
European Hazard Symbols
GHS Pictograms
GHS Hazard statements
Risk Statements
German water hazard class
Storage Temperature
TSCA Listed
Certificate of Analysis
Purity
Empirical Formula (Hill Notation)
Melting Point
Flash Point
Boiling Point