KBR2738
KBR2738 structure
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Common Name | KBR2738 | ||
|---|---|---|---|---|
| CAS Number | 126833-17-8 | Molecular Weight | 302.20 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 457.9±45.0 °C at 760 mmHg | |
| Molecular Formula | C14H17Cl2NO2 | Melting Point | 153ºC | |
| MSDS | Chinese USA | Flash Point | 230.7±28.7 °C | |
| Symbol |
GHS09 |
Signal Word | ||
Use of KBR2738Fenhexamid, a botryticide, is a sterol biosynthesis inhibitor. Fenhexamid shows fungicide efficient against the plant pathogenic fungus Botryotinia fuckeliana (Botrytis cinerea)[1]. |
| Name | fenhexamid |
|---|---|
| Synonym | More Synonyms |
| Description | Fenhexamid, a botryticide, is a sterol biosynthesis inhibitor. Fenhexamid shows fungicide efficient against the plant pathogenic fungus Botryotinia fuckeliana (Botrytis cinerea)[1]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 457.9±45.0 °C at 760 mmHg |
| Melting Point | 153ºC |
| Molecular Formula | C14H17Cl2NO2 |
| Molecular Weight | 302.20 |
| Flash Point | 230.7±28.7 °C |
| Exact Mass | 301.063629 |
| PSA | 49.33000 |
| LogP | 4.02 |
| Vapour Pressure | 0.0±1.2 mmHg at 25°C |
| Index of Refraction | 1.604 |
| InChIKey | VDLGAVXLJYLFDH-UHFFFAOYSA-N |
| SMILES | CC1(C(=O)Nc2ccc(O)c(Cl)c2Cl)CCCCC1 |
| Symbol |
GHS09 |
|---|---|
| Hazard Statements | H411 |
| Precautionary Statements | P273-P391-P501 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Risk Phrases | R51/53 |
| Safety Phrases | S61 |
| RIDADR | UN 3077 9/PG 3 |
| RTECS | GU7879550 |
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Simultaneous determination of sixteen amide fungicides in vegetables and fruits by dispersive solid phase extraction and liquid chromatography-tandem mass spectrometry.
J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 989 , 11-20, (2015) A modified quick, easy, cheap, effective, rugged, and safe (QuEChERS) method using multi-walled carbon nanotubes (MWCNTs) as a reversed-dispersive solid phase extraction (r-dSPE) material combined wit... |
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The effects of the fungicides fenhexamid and myclobutanil on SH-SY5Y and U-251 MG human cell lines.
Environ. Toxicol. Pharmacol. 38(3) , 968-76, (2014) Mixtures of pesticides in foodstuffs and the environment are ubiquitous in the developed world and although agents are usually exhaustively tested individually, the toxicological implications of pesti... |
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Fungicide-driven evolution and molecular basis of multidrug resistance in field populations of the grey mould fungus Botrytis cinerea.
PLoS Pathog. 5 , e1000696, (2009) The grey mould fungus Botrytis cinerea causes losses of commercially important fruits, vegetables and ornamentals worldwide. Fungicide treatments are effective for disease control, but bear the risk o... |
| MFCD03095700 |
| 2’,3’-dichloro-4’-hydroxy-1-methylcyclohexanecarboxanilide |
| N-(2,3-dichloro-4-hydroxyphenyl)-1-methylcyclohexane-1-carboxamide |
| EINECS 422-530-5 |
| Fenhexamid |
| N-(2,3-Dichloro-4-hydroxyphenyl)-1-methylcyclohexanecarboxamide |
| KBR2738 |
| KBR-2738 |
| L6TJ AVMR DQ BG CG& A1 |