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Molecule
ID:59183
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₆N₂O₂
Molecular Mass
138.12404
Exact Mass
138.04292744
Charge
0
InChI
InChI=1S/C6H6N2O2/c1-10-6(9)5-4-7-2-3-8-5/h2-4H,1H3
InChIKey
TWIIRMSFZNYMQE-UHFFFAOYSA-N
Canonic Smiles
COC(=O)c1cnccn1
Isomeric Smiles
c1cncc(n1)C(=O)OC
Calculated Properties
JChem
H Acceptors
3
H Donor
0
LogD (pH = 5.5)
-0.27277187
LogD (pH = 7.4)
-0.27277175
Log P
-0.27277175
Molar Refractivity
33.3975
Polarizability
13.024475
Polar Surface Area
52.08
Rotatable Bonds
2
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
•
IUPAC name
•
Synonyms
Registration numbers
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
OR6399
Sigma Aldrich
519677
Matrix Scientific
064371
Enamine
EN300-100508
Bide Pharmatech
BD3516
Alfa Aesar
A12028
A&J Pharmtech
AJA-O14588
Academic Data
PubChem
72662
Names and Identifiers
IUPAC Traditional name
2-methylpyrazine carboxylate
IUPAC name
methyl pyrazine-2-carboxylate
Synonyms
Methyl pyrazine-2-carboxylate
Methyl pyrazine-2-carboxylate 98%
Methyl 2-pyrazinecarboxylate
2-吡嗪羧酸甲酯
Methyl 2-pyrazinecarboxylate
Methyl pyrazine-2-carboxylate
Methyl pyrazinoate
Pyrazine-2-carboxylic acid methyl ester
吡嗪-2-羧酸甲酯
Registration numbers
CAS Number
6164-79-0
MDL Number
MFCD00014611
Merck Index
147959
Beilstein Number
118345
EC Number
228-198-6
PubChem SID
162063946
24873927
PubChem CID
72662
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
是
Source
MSDS Link
Download link
Source
Download link
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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
Risk Statements
36/37/38
Source
Safety Statements
26
-
36
Source
26
-
37
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
German water hazard class
3
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Signal Word
Warning
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Physical Property
Melting Point
57-61°C
Source
57-61 °C(lit.)
Source
59 - 61°C
Source
56-60°C
Source
Hydrophobicity(logP)
-0.673
Source
Flash Point
>100°C(212°F)
Source
Product Information
Empirical Formula (Hill Notation)
C6H6N2O2
Source
Purity
97%
Source
95%
Source
98%
Source
98+%
Source
Molecule Details
Sigma Aldrich
519677
Packaging
5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
Merck Index
•
Beilstein Number
•
EC Number
•
PubChem SID
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PubChem CID