CAS Number67564-91-4
Synonymscis-4-<3-(4-tert-butylphenyl)-2-methylpropyl>-2,6-dimethylmorpholine; 4,10-dioxatricyclo[5.2.1.0<2,6>]decan-3,5-dione; Wln: T C555 A ao dvovtj; demethylcantharidin; (2R,6S)-rel-4-[3-[4-(1,1-dimethylethyl)phenyl]-2-methylpropyl]-2,6-dimethylmorpholine; rac-(2R,6S)-4-[(2Ξ)-3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine; 3,6-Endooxyphthalic anhydride,hexahydro; MFCD00144306; rel-(2R,6S)-4-[3-[4-(1,1-dimethylethyl)phenyl]-2-methylpropyl]-2,6-dimethylmorpholine; hexahydro-4,7-epoxyisobenzofuran-1,3-dione; 7-oxabicyclo[2,2,1]heptane-2,3-dicarboxylic acid anhydride; cis-exo-hexahydro-4,7-epoxyisobenzofuran-1,3-dione; 4-[3-(4-tert-butyl-phenyl)-2-methyl-propyl]-2,6-dimethyl-morpholine; EINECS 266-719-9; Fenpropimorph; Demehylcantharidin; cis-4-[(RS)-3-(4-tert-butylphenyl)-2-methylpr
Molecular FormulaC20H33NO
Molecular Weight303.48
Purity98.00%
Density0.928 g/cm3
Boiling Point392.7ºC at 760 mmHg
Melting Point25°C
Appearanceliquid
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 67564-91-4 |
| Catalog No. | 2A-1186742 |
| Chinese Name | 顺-4-叔丁基苯基(-2-甲基丙基)-2,6-二甲基吗啉 |
| Synonyms | cis-4-<3-(4-tert-butylphenyl)-2-methylpropyl>-2,6-dimethylmorpholine; 4,10-dioxatricyclo[5.2.1.0<2,6>]decan-3,5-dione; Wln: T C555 A ao dvovtj; demethylcantharidin; (2R,6S)-rel-4-[3-[4-(1,1-dimethylethyl)phenyl]-2-methylpropyl]-2,6-dimethylmorpholine; rac-(2R,6S)-4-[(2Ξ)-3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine; 3,6-Endooxyphthalic anhydride,hexahydro; MFCD00144306; rel-(2R,6S)-4-[3-[4-(1,1-dimethylethyl)phenyl]-2-methylpropyl]-2,6-dimethylmorpholine; hexahydro-4,7-epoxyisobenzofuran-1,3-dione; 7-oxabicyclo[2,2,1]heptane-2,3-dicarboxylic acid anhydride; cis-exo-hexahydro-4,7-epoxyisobenzofuran-1,3-dione; 4-[3-(4-tert-butyl-phenyl)-2-methyl-propyl]-2,6-dimethyl-morpholine; EINECS 266-719-9; Fenpropimorph; Demehylcantharidin; cis-4-[(RS)-3-(4-tert-butylphenyl)-2-methylpr |
| Molecular Formula | C20H33NO |
| Molecular Weight | 303.48 |
| Purity | 98.00 |
| Density | 0.928 g/cm3 |
| Boiling Point | 392.7ºC at 760 mmHg |
| Melting Point | 25°C |
| Appearance | liquid |
| Storage Condition | 2-8°C, sealed |
| Application | Fenpropimorph is a fungicide that inhibits the sterol pathway. Fenpropimorph inhibits δ8-δ7-sterol isomerase in yeast at low concentrations and δ14-sterol reductase at high concentrations, preventing |
| PubChem ID | 11102488 |
| SMILES | CC(Cc1ccc(C(C)(C)C)cc1)CN1CC(C)OC(C)C1 |
| InChI | InChI=1S/C20H33NO/c1-15(12-21-13-16(2)22-17(3)14-21)11-18-7-9-19(10-8-18)20(4,5)6/h7-10,15-17H,11-14H2,1-6H3/t15?,16-,17+ |
| InChI Key | RYAUSSKQMZRMAI-ALOPSCKCSA-N |
| Hazard Symbols | transportation |
| Bioactivity | Fenpropimorph is a fungicide that inhibits the sterol pathway. Fenpropimorph inhibits δ8-δ7-sterol isomerase in yeast at low concentrations, with δ14-sterol reductase being blocked at higher levels, preventing the biosynthesis of ergosterol. Fenpropimorph also inhibits sterol synthesis in certain plants and mammalian cells[1][2][3]. Related Catalog Research Areas >> Infection Signaling Pathways >> Anti-infection >> Fungal References [1]. Costet MF, et al. Ecdysteroid biosynthesis and embryonic development are disturbed in insects (Locusta migratoria) reared on plant diet (Triticum sativum) with a selectively modified sterol profile. Proc Natl Acad Sci U S A. 1987;84(3):643-647. [2]. Marcireau C, et al. In vivo effects of fenpropimorph on the yeast Saccharomyces cerevisiae and determination of the molecular basis of the antifungal property. Antimicrob Agents Chemother. 1990;34(6):989-993. [3]. Corio-Costet MF, et al. Inhibition by the fungicide fenpropimorph of cholesterol biosynthesis in 3T3 fibroblasts. Biochem J. 1988;256(3):829-834. Chemical & Physical Properties Density 0.928 g/cm3 Boiling Point 392.7ºC at 760 mmHg Melting Point 25°C Molecular Formula C20H33NO Molecular Weight 303.48 Flash Point 115.6ºC Exact Mass 303.25600 PSA 12.47000 LogP 4.20980 Index of Refraction 1.49 InChIKey RYAUSSKQMZRMAI-ALOPSCKCSA-N SMILES CC(Cc1ccc(C(C)(C)C)cc1)CN1CC(C)OC(C)C1 |
| Use of | Fenpropimorph is a fungicide that inhibits the sterol pathway. Fenpropimorph inhibits δ8-δ7-sterol isomerase in yeast at low concentrations, with δ14-sterol reductase being blocked at higher levels, preventing the biosynthesis of ergosterol. Fenpropimorph also inhibits sterol synthesis in certain plants and mammalian cells[1][2][3]. Properties Name fenpropimorph Synonym More Synonyms Fenpropimorph Biological Activity Description Fenpropimorph is a fungicide that inhibits the sterol pathway. Fenpropimorph inhibits δ8-δ7-sterol isomerase in yeast at low concentrations, with δ14-sterol reductase being blocked at higher levels, preventing the biosynthesis of ergosterol. Fenpropimorph also inhibits sterol synthesis in certain plants and mammalian cells[1][2][3]. Related Catalog Research Areas >> Infection Signaling Pathways >> Anti-infection >> Fungal References [1]. Costet MF, et al. Ecdysteroid biosynthesis and embryonic development are disturbed in insects (Locusta migratoria) reared on plant diet (Triticum sativum) with a selectively modified sterol profile. Proc Natl Acad Sci U S A. 1987;84(3):643-647. [2]. Marcireau C, et al. In vivo effects of fenpropimorph on the yeast Saccharomyces cerevisiae and determination of the molecular basis of the antifungal property. Antimicrob Agents Chemother. 1990;34(6):989-993. [3]. Corio-Costet MF, et al. Inhibition by the fungicide fenpropimorph of cholesterol biosynthesis in 3T3 fibroblasts. Biochem J. 1988;256(3):829-834. Chemical & Physical Properties Molecular Formula C20H33NO Exact Mass 303.25600 PSA 12.47000 LogP 4.20980 Index of Refraction 1.49 InChIKey RYAUSSKQMZRMAI-ALOPSCKCSA-N |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Danger Regulations: 3082 International Maritime Danger Regulations: 3082 International Air Transport Danger Regulations: 3082 14.2 Names specified by the United Nations (UN) European land transport hazard regulations: ENVIRONMENTALLY HAZARDOUS SUBSTANCE, LIQUID, N.O.S. (Fenpropimorph) IMDG: ENVIRONMENTALLY HAZARDOUS SUBSTANCE, LIQUID, N.O.S. (Fenpropimorph) International air transport hazard regulations: Environmentally hazardous substance, liquid, n.o.s. (Fenpropimorph) 14.3 Transport hazard categories European land transport Dangerous Regulations: 9 International sea transport Dangerous Regulations: 9 International air transport Dangerous Regulations: 9 14.4 Package group European Land Transport Danger Regulations: III International Maritime Transport Danger Regulations: III International Air Transport Danger Regulations: III 14.5 Environmental hazards European Land Transport Dangerous Regulations: Yes International Maritime Transport Dangerous Regulations Maritime Pollutants: Yes International Air Transport Dangerous Regulations: Yes 14.6 Special reminder to users further information Dangerous goods are individually packaged, with liquids exceeding 5 liters or solids exceeding 5 kilograms. The outer packaging of each independent package and the combined independent inner package must have EHS on it. Identification (according to European ADR Regulation 2.2.9.1.10, IMDG Regulation 2.10.3), |
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