Dimethomorph (CAS 110488-70-5) — formula C21H22ClNO4, molecular weight 387.9.
| CAS Number | 110488-70-5 |
|---|---|
| Molecular Formula | C21H22ClNO4 |
| Molecular Weight | 387.9 |
| Melting Point | 127-148 °C |
| LogP | 3.9 |
| Applications | Uses: Used as agricultural fungicide, [Merck Index] Used as a systemic fungicide on potatoes, [Reference #1], Farming (Pesticides) [Category: Industry], For dimethomorph (USEPA, OPP Pesticide Code: 268800) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Fungicide effective against Oomycetes, especially Peronosporaceae and Phytophthora spp. (but not Pythium spp.) in vines, potatoes and tomatoes. Used in combination with contact fungicides., Fungicide, This is a man-made compound that is used as a pesticide., Use Classification: Fungicides, Methods of Manufacturing: Dimethomorph is produced by Friedel-Crafts acylation of 1, 2-dimethoxybenzene with 4-chlorobenzoyl chloride, followed by condensation with triethyl phosphonoacetate in the presence of a base such as sodium hydride in dimethoxyethane. The resulting ethyl cinnamate is then converted to the correspondingmorpholide., Formulations, Preparations: Premix Partners: Ametoctradin, Chlorothalonil, Copper sulfate, tribasic, Folpet, Mancozeb., Dispersible concentrate, suspension concentrate, wettable powder., Composition: (E) isomer to (Z) isomer ratio is 1:1., Acrobat(R) Fungicide Technical (BASF Corporation), Dimethomorph 98.98%., For more Formulations, Preparations (Complete) data for DIMETHOMORPH (15 total), please visit the HSDB record page., General Manufacturing Information: The WHO Recommended Classification of Pesticides by Hazard identifies dimethomorph (technical grade) as Class III: slightly hazardous, Main Use: fungicide, other than for seed treatment., Fungicidal activity is primarily associated with the Z isomer., Only the (Z)- isomer is intrinsically active, but, because of rapid interconversion of isomers in the light, it has no advantage over the (E)-isomer in practice. |
Documented applications: Uses: Used as agricultural fungicide, [Merck Index] Used as a systemic fungicide on potatoes, [Reference #1], Farming (Pesticides) [Category: Industry], For dimethomorph (USEPA, OPP Pesticide Code: 268800) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Fungicide effective against Oomycetes, especially Peronosporaceae and Phytophthora spp. (but not Pythium spp.) in vines, potatoes and tomatoes. Used in combination with contact fungicides., Fungicide, This is a man-made compound that is used as a pesticide., Use Classification: Fungicides, Methods of Manufacturing: Dimethomorph is produced by Friedel-Crafts acylation of 1, 2-dimethoxybenzene with 4-chlorobenzoyl chloride, followed by condensation with triethyl phosphonoacetate in the presence of a base such as sodium hydride in dimethoxyethane. The resulting ethyl cinnamate is then converted to the correspondingmorpholide., Formulations, Preparations: Premix Partners: Ametoctradin, Chlorothalonil, Copper sulfate, tribasic, Folpet, Mancozeb., Dispersible concentrate, suspension concentrate, wettable powder., Composition: (E) isomer to (Z) isomer ratio is 1:1., Acrobat(R) Fungicide Technical (BASF Corporation), Dimethomorph 98.98%., For more Formulations, Preparations (Complete) data for DIMETHOMORPH (15 total), please visit the HSDB record page., General Manufacturing Information: The WHO Recommended Classification of Pesticides by Hazard identifies dimethomorph (technical grade) as Class III: slightly hazardous, Main Use: fungicide, other than for seed treatment., Fungicidal activity is primarily associated with the Z isomer., Only the (Z)- isomer is intrinsically active, but, because of rapid interconversion of isomers in the light, it has no advantage over the (E)-isomer in practice..
Dimethomorph is a chemical compound with CAS registry number 110488-70-5 and molecular formula C21H22ClNO4 (molecular weight 387.9).
CAS number: 110488-70-5
Its molecular formula C21H22ClNO4 comprises 21 C, 22 H, 1 Cl, 1 N, 4 O atoms.
Also known as: Dimethomorph · 烯酰吗啉
The CAS registry number of Dimethomorph is 110488-70-5.
Molecular formula C21H22ClNO4, molecular weight 387.9.
It is also registered under: Dimethomorph, 烯酰吗啉.
Recorded applications: Uses: Used as agricultural fungicide, [Merck Index] Used as a systemic fungicide on potatoes, [Reference #1], Farming (Pesticides) [Category: Industry], For dimethomorph (USEPA, OPP Pesticide Code: 268800) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Fungicide effective against Oomycetes, especially Peronosporaceae and Phytophthora spp. (but not Pythium spp.) in vines, potatoes and tomatoes. Used in combination with contact fungicides., Fungicide, This is a man-made compound that is used as a pesticide., Use Classification: Fungicides, Methods of Manufacturing: Dimethomorph is produced by Friedel-Crafts acylation of 1, 2-dimethoxybenzene with 4-chlorobenzoyl chloride, followed by condensation with triethyl phosphonoacetate in the presence of a base such as sodium hydride in dimethoxyethane. The resulting ethyl cinnamate is then converted to the correspondingmorpholide., Formulations, Preparations: Premix Partners: Ametoctradin, Chlorothalonil, Copper sulfate, tribasic, Folpet, Mancozeb., Dispersible concentrate, suspension concentrate, wettable powder., Composition: (E) isomer to (Z) isomer ratio is 1:1., Acrobat(R) Fungicide Technical (BASF Corporation), Dimethomorph 98.98%., For more Formulations, Preparations (Complete) data for DIMETHOMORPH (15 total), please visit the HSDB record page., General Manufacturing Information: The WHO Recommended Classification of Pesticides by Hazard identifies dimethomorph (technical grade) as Class III: slightly hazardous, Main Use: fungicide, other than for seed treatment., Fungicidal activity is primarily associated with the Z isomer., Only the (Z)- isomer is intrinsically active, but, because of rapid interconversion of isomers in the light, it has no advantage over the (E)-isomer in practice..
Independent reference data for Dimethomorph (CAS 110488-70-5), compiled from public chemistry databases.
| CAS Registry Number | 110488-70-5 |
|---|---|
| PubChem CID | 86298 |
| Molecular formula | C21H22ClNO4 |
| IUPAC name | 3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-morpholin-4-ylprop-2-en-1-one |
| UNII (FDA) | 3EXL2158GV |
| Molecular Weight | 387.9 |
|---|---|
| XLogP3 | 3.9 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 5 |
| Exact Mass | 387.1237359 |
| Monoisotopic Mass | 387.1237359 |
| Topological Polar Surface Area | 48 |
| Heavy Atom Count | 27 |
| Melting Point | 127-148 °C |
|---|---|
| Melting Point | MP: 125-149 °C |
| Vapor Pressure | 0.00000001 [mmHg] |
| Vapor Pressure | 7.39X10-6 mm Hg at 25 °C |
Dimethomorph; 110488-70-5; DTXSID7034545; Acrobat; 3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-morpholin-4-ylprop-2-en-1-one; Akrobat; Forum; Festival C; CME 151; 3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-(morpholin-4-yl)prop-2-en-1-one; 3EXL2158GV; DTXCID5014545; CHEBI:81848; Athlete; 4-(3-(4-Chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-oxo-2-propenyl)morpholine; 2-Propen-1-one, 3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-(4-morpholinyl)-
| Reported hazard statements | H411, H401, H410, H360 |
|---|
H360F: May damage fertility [Danger Reproductive toxicity]
H411: Toxic to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard]
Dimethomorph · CAS 110488-70-5 · C21H22ClNO4. UNII 3EXL2158GV. Melting Point: 127-148 °C; Melting Point: MP: 125-149 °C; Vapor Pressure: 0.00000001 [mmHg].
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: 烯酰吗啉