![Methyl[[2-chloro-5-[(1E)-1-[[(6-methyl-2-pyridinyl)methoxy]imino]ethyl]phenyl]methyl]carbamate structure, CAS 799247-52-2](/structures/80000/70318_1_799247_52_2.png)
CAS Number799247-52-2
SynonymsPyribencarb; methyl {2-chloro-5-[(1E)-1-(6-methyl-2-pyridylmethoxyimino)ethyl]benzyl}carbamate; methyl [(2-chloro-5-{(1E)-N-[(6-methylpyridin-2-yl)methoxy]ethanimidoyl}phenyl)methyl]carbamate; methyl N-[[2-chloro-5-[(1E)-1-[[(6-methyl-2-pyridinyl)methoxy]imino]ethyl]phenyl]methyl]carbamate
Molecular FormulaC18H20ClN3O3
Molecular Weight361.82
Density1.221g/cm3
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 799247-52-2 |
| Catalog No. | 2A-9070318 |
| Chinese Name | 吡菌苯威 |
| Synonyms | Pyribencarb; methyl {2-chloro-5-[(1E)-1-(6-methyl-2-pyridylmethoxyimino)ethyl]benzyl}carbamate; methyl [(2-chloro-5-{(1E)-N-[(6-methylpyridin-2-yl)methoxy]ethanimidoyl}phenyl)methyl]carbamate; methyl N-[[2-chloro-5-[(1E)-1-[[(6-methyl-2-pyridinyl)methoxy]imino]ethyl]phenyl]methyl]carbamate |
| Molecular Formula | C18H20ClN3O3 |
| Molecular Weight | 361.82 |
| Density | 1.221g/cm3 |
| Storage Condition | 2-8°C |
| Application | Pyribencarb is a benzyl carbamate-type fungicide active against a variety of plant pathogenic fungi. Pyribencarb is a potent Qo inhibitor of cytochrome b. Pyribencarb is particularly effective against |
| PubChem ID | 24261666 |
| SMILES | COC(=O)NCc1cc(C(C)=NOCc2cccc(C)n2)ccc1Cl |
| InChI | InChI=1S/C18H20ClN3O3/c1-12-5-4-6-16(21-12)11-25-22-13(2)14-7-8-17(19)15(9-14)10-20-18(23)24-3/h4-9H,10-11H2,1-3H3,(H,20,23)/b22-13+ |
| InChI Key | CRFYLQMIDWBKRT-LPYMAVHISA-N |
| Hazard Symbols | transportation |
| Bioactivity | Pyribencarb is a benzylcarbamate-type fungicide, which is active against a wide range of plant pathogenic fungi. Pyribencarb is a potent Qo inhibitor of cytochrome b. Pyribencarb is especially active against Botrytis cinerea and Sclerotinia sclerotirum[1]. Related Catalog Research Areas >> Infection Signaling Pathways >> Anti-infection >> Fungal In Vitro Pyribencarb potently inhibits succinate-cytochrome c reductase (SCR) activities of Botrytis cinerea (cucumber gray mold), Corynespora cassiicola (leaf spot) and decylubiquinol-cytochrome c reductase (UCR) activity of B. cinerea. Pyribencarb inhibits the UCR of B. cinerea in an uncompetitive manner, and the substrate-dependent inhibition constant is found from calculation to be 13 nM[1]. The target site of Pyribencarb is cytochrome b of complex III in the electron transport system of the respiratory chain. The inhibitory potency of pyribencarb on SCR activities of plants, rats and carp is relatively weak compared with that of strobilurin fungicides[1]. References [1]. Satoshi Kataoka, et al. Mechanism of action and selectivity of a novel fungicide, pyribencarb. J Pestic Sci, 35(2), 99-106 (2010). Chemical & Physical Properties Density 1.221g/cm3 Molecular Formula C18H20ClN3O3 Molecular Weight 361.82300 Exact Mass 361.11900 PSA 76.30000 LogP 4.04460 Index of Refraction 1.57 InChIKey CRFYLQMIDWBKRT-LPYMAVHISA-N SMILES COC(=O)NCc1cc(C(C)=NOCc2cccc(C)n2)ccc1Cl Storage condition 2-8°C |
| Use of | Pyribencarb is a benzylcarbamate-type fungicide, which is active against a wide range of plant pathogenic fungi. Pyribencarb is a potent Qo inhibitor of cytochrome b. Pyribencarb is especially active against Botrytis cinerea and Sclerotinia sclerotirum[1]. Properties Name pyribencarb Synonym More Synonyms Pyribencarb Biological Activity Description Pyribencarb is a benzylcarbamate-type fungicide, which is active against a wide range of plant pathogenic fungi. Pyribencarb is a potent Qo inhibitor of cytochrome b. Pyribencarb is especially active against Botrytis cinerea and Sclerotinia sclerotirum[1]. Related Catalog Research Areas >> Infection Signaling Pathways >> Anti-infection >> Fungal In Vitro Pyribencarb potently inhibits succinate-cytochrome c reductase (SCR) activities of Botrytis cinerea (cucumber gray mold), Corynespora cassiicola (leaf spot) and decylubiquinol-cytochrome c reductase (UCR) activity of B. cinerea. Pyribencarb inhibits the UCR of B. cinerea in an uncompetitive manner, and the substrate-dependent inhibition constant is found from calculation to be 13 nM[1]. The target site of Pyribencarb is cytochrome b of complex III in the electron transport system of the respiratory chain. The inhibitory potency of pyribencarb on SCR activities of plants, rats and carp is relatively weak compared with that of strobilurin fungicides[1]. References [1]. Satoshi Kataoka, et al. Mechanism of action and selectivity of a novel fungicide, pyribencarb. J Pestic Sci, 35(2), 99-106 (2010). Chemical & Physical Properties Exact Mass 361.11900 PSA 76.30000 LogP 4.04460 Index of Refraction 1.57 InChIKey CRFYLQMIDWBKRT-LPYMAVHISA-N |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available |
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