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Molecule
ID:6834
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₄H₄ClN₃
Molecular Mass
129.54766
Exact Mass
129.00937482
Charge
0
InChI
InChI=1S/C4H4ClN3/c5-3-1-7-4(6)8-2-3/h1-2H,(H2,6,7,8)
InChIKey
OQZMDDKDHRIGDY-UHFFFAOYSA-N
Canonic Smiles
Clc1cnc(nc1)N
Isomeric Smiles
c1(ncc(cn1)Cl)N
Calculated Properties
JChem
Acid pKa
16.584192
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
0.50331193
LogD (pH = 7.4)
0.50363606
Log P
0.5036402
Molar Refractivity
32.1735
Polarizability
11.639226
Polar Surface Area
51.8
Rotatable Bonds
0
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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Quote
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
Synonyms
•
IUPAC Traditional name
•
IUPAC name
Registration numbers
Properties
•
Product Information
•
Safety Information
•
Physical Property
Related Proteins
Molecular Spectra
Molecule Details
•
MP Biomedicals
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Names and Identifiers
Synonyms
5-Chloro-2-pyrimidinamine
2-Amino-5-chloropyrimidine
2-氨基-5-氯嘧啶
2-Amino-5-chloropyrimidine
5-chloropyrimidin-2-amine
5-Chloro-2-pyrimidinamine
5-chloro-pyrimidin-2-ylamine
IUPAC Traditional name
5-chloropyrimidin-2-amine
IUPAC name
5-chloropyrimidin-2-amine
Registration numbers
EC Number
226-581-2
CAS Number
5428-89-7
MDL Number
MFCD00014604
Beilstein Number
110914
PubChem SID
24883840
160970141
PubChem CID
79479
Molecule Details
MP Biomedicals
05222384
MP Biomedicals Rare Chemical collection
Sigma Aldrich
651567
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
EC Number
•
CAS Number
•
MDL Number
•
Beilstein Number
•
PubChem SID
•
PubChem CID
Data Source
Commercial Catalog
Apollo Scientific
OR4453
Matrix Scientific
001651
MP Biomedicals
05222384
Key Organics
8P-009
Sigma Aldrich
651567
Properties
Product Information
Purity
98%
Source
>95%
Source
97%
Source
95%
Source
Certificate of Analysis
Download link
Source
Empirical Formula (Hill Notation)
C4H4ClN3
Source
Safety Information
Download link
Source
Download link
Source
Download link
Source
false
Source
是
Source
Physical Property
235°C
Source
235-241°C
Source
230 - 234 °C
Source
235-238 °C(lit.)
Source
235 - 238°C
Source
235°C
Source
0.435
Source
Alfa Aesar
L19248
Bide Pharmatech
BD2223
Enamine
EN300-95739
A&J Pharmtech
AJA-O12456
AJA-O38479
Academic Data
PubChem
79479
Storage Warning
Irritant
Source
Safety Statements
S:
9
-
16
-
29
Source
26
-
36/37
Source
26
-
37
Source
European Hazard Symbols
Flammable (F)
Source
Harmful (Xn)
Irritant (Xi)
Risk Statements
R:
10
Source
22
-
41
Source
36/37/38
Source
RTECS
UV6329500
Source
Hazard Class
6.1
Source
RID/ADR
UN 2811 6.1/PG 3
Source
GHS Hazard statements
H301
-
H318
Source
H315
-
H319
-
H335
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Source
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
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
GHS Signal Word
Danger
Source
UN Number
2811
Source
German water hazard class
3
Source
Packing Group
3
Source
GHS Precautionary statements
P280
-
P301+P310
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
MSDS Link
TSCA Listed
Melting Point
Hydrophobicity(logP)
Source
Source
Source
Source