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Details
Bulk supply high purity IPCONAZOLE 125225-28-7, Paid sample available
- Molecular Formula: C18H24 Cl N3 O
- Molecular Weight: 333.861
- Vapor Pressure: 2.94E-10mmHg at 25°C
- Melting Point: 86～92℃
- Boiling Point: 486°Cat760mmHg
- PKA: 13.76±0.60(Predicted)
- Flash Point: 247.7°C
- PSA： 50.94000
- Density: 1.24g/cm3
- LogP: 3.58750
IPCONAZOLE(Cas 125225-28-7) Usage
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Metabolic pathway |
Ipconazole is a mixture of two geometric isomer pairs (lRS,2SR,5RS) (I) and (lRS,2SR,5SR) (Ⅱ). They differ in the orientation of the hydroxy, benzyl and isopropyl groups. The ratio of I : II in the technical product is 90 : 10 and the two-component isomer pairs are of equal activity. The metabolism of ipconazole in plants and animals involves oxidation at the benzylic and isopropyl groups to yield alcohols which may be further oxidised to the corresponding ketones or carboxylic acids (or lactones). The resulting array of metabolites can be expected to be stereochemically more complex than the original isomer mixture. |
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Degradation |
Ipconazole is stable towards hydrolysis and is thermally stable. |
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Definition |
ChEBI: A member of the class of cyclopentanols carrying 1,2,4-triazol-1-ylmethyl, 4-chlorobenzyl and isopropyl substituents at positions 1, 2 and 5 respectively. Used to control a range of seed diseases in rice, vegetables and other, mainly non-food, crops. |
InChI:InChI=1/C18H24ClN3O/c1-13(2)17-8-5-15(9-14-3-6-16(19)7-4-14)18(17,23)10-22-12-20-11-21-22/h3-4,6-7,11-13,15,17,23H,5,8-10H2,1-2H3
125225-28-7 Relevant articles
Synthesis method of triazole bactericide
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Paragraph 0035-0036, (2020/10/14)
The invention relates to a triazole bact...
METHOD FOR PRODUCING TRIAZOLYL METHYL CYCLOALKANOL DERIVATIVE AND TRIAZOLYL METHYL CYCLOALKANOL DERIVATIVE-CONTAINING COMPOSITION
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Paragraph 0057; 0058; 0061, (2015/03/16)
Generation of by-product is reduced by p...
Synergistic Active Compound Combinations Comprising Phenyltriazoles
-
, (2011/07/29)
The present invention relates to novel a...
Process for preparation of azolylmethylcycloalkanol derivatives
-
, (2008/06/13)
A process for preparing a derivative of ...
125225-28-7 Process route
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2-(4-chlorobenzyl)-5-(1-methylethyl)cyclopentanone
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41253-21-8
sodium triazole
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25596-24-1
trimethyloxosulfonium bromide
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-
125225-28-7
ipconazole
| Conditions | Yield |
|---|---|
|
With
sodium hydroxide;
In
1-methyl-pyrrolidin-2-one;
at 100 ℃;
for 11h;
Flow reactor;
|
78%
|
-
-
2-(4-chlorobenzyl)-5-(1-methylethyl)cyclopentanone
-
-
41253-21-8
sodium triazole
-
-
125225-28-7
ipconazole
| Conditions | Yield |
|---|---|
|
With
trimethylsulphonium bromide; sodium t-butanolate;
In
1-methyl-pyrrolidin-2-one;
at 115 ℃;
for 1h;
Inert atmosphere;
|
1.24%
|
125225-28-7 Upstream products
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288-88-0
1,2,4-Triazole
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872-50-4
1-methyl-pyrrolidin-2-one
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25596-24-1
trimethyloxosulfonium bromide
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41253-21-8
sodium triazole
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