4-Amino-2-chloropyridine
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4-Amino-2-chloropyridine
structure -
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CAS No:
14432-12-3
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Formula:
C5H5ClN2
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Chemical Name:
4-Amino-2-chloropyridine
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Synonyms:
4-Pyridinamine,2-chloro-;Pyridine,4-amino-2-chloro-;2-Chloro-4-pyridinamine;4-Amino-2-chloropyridine;2-Chloro-4-aminopyridine;(2-Chloropyridin-4-yl)amine;2-Chloropyridin-4-amine
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CAS No:
Description
White powder.4-Amino-2-chloropyridine is an important pharmaceutical and pesticide intermediate. It can synthesize N-(2-chloro-4-pyridyl)urea regulators that promote plant growth. It is also a key substance in the synthesis of KT-30 (Forchlorfenuron, IUPAC name N-(2-chloro-4-pyridyl)-N'-phenylurea). KT-30 is a highly active cytokinin, which has the biological activity of promoting tissue growth, promoting bud development and green preservation; it has an effect of increasing yield on apple, pea
4-Amino-2-chloropyridine is an aminopyridine.
4-Amino-2-chloropyridine Basic Attributes
128.56
128.56
108671
238-403-0
BHC29VF8KH
DTXSID20162674
29333999
Characteristics
38.9
1.1
Light yellow Crystalline Powder
1.2417 (rough estimate)
91-91.5 °C
153°C5mm
153°C/5mm
1.5110 (estimate)
Slightly soluble in water.
Store in a cool, dry place. Store in a tightly closed container.
0.00116mmHg at 25°C
Safety Information
IRRITANT
2811
3
36/37/38
26-36-37/39-36/37/39
Xi
Irritant
P261-P305 + P351 + P338
H315-H319-H335
|Warning|H302 (15.69%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 51 companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
4-Amino-2-chloropyridine Use and Manufacturing
The preparation method uses isonicotinic acid as a raw material, chlorination with phosphorus oxychloride to obtain 2-chloropyridine-4-carboxylic acid, and then reacts with ammonia gas to form a corresponding amide, and then undergoes Huffman degradation reaction to obtain a product . You can also use 2-chloropyridine-N-oxide as the raw material, first nitrate with fuming nitric acid, and then reduce it with iron powder in acetic acid to obtain the product.
An aminopyridine derivative with potential herbicidal activity.
Computed Properties
Molecular Weight:128.56
XLogP3:1.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Exact Mass:128.0141259
Monoisotopic Mass:128.0141259
Topological Polar Surface Area:38.9
Heavy Atom Count:8
Complexity:76.8
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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