| Identification | Back Directory | [Name]
Mandipropamid | [CAS]
374726-62-2 | [Synonyms]
noa 446510
Mandipropamid
Mandipropamid [iso]
Mandipropamid Standard
Mandipropamid Solution, 1000ppm
MandipropamidSolution,100mg/L,1ml
Mandipropamid@100 μg/mL in Acetonitrile
Mandipropamid@1000 μg/mL in Acetonitrile
Mandipropamid Solution in Acetonitrile, 1000μg/mL
2-(4-Chlorophenyl)-N-[3-methoxy-4-(2-propynyloxy)phenethyl]-2-(2-propynyloxy)acetamide
2-(4-Chlorophenyl)-N-[2-[3-methoxy-4-(prop-2-ynyloxy)phenyl]ethyl]-2-(prop-2-ynyloxy)acetamide
2-(4-chlorophenyl)-N-(2-Methoxy-4-(prop-2-yn-1-yloxy)phenethyl)-2-(prop-2-yn-1-yloxy)acetaMide
Benzeneacetamide,4-chloro-N-[2-[3-methoxy-4-(2-propyn-1-yloxy)phenyl]ethyl]-a-(2-propyn-1-yloxy)-
Benzeneacetamide, 4-chloro-N-[2-[3-methoxy-4-(2-propyn-1-yloxy)phenyl]ethyl]-α-(2-propyn-1-yloxy)- | [Molecular Formula]
C23H22ClNO4 | [MOL File]
374726-62-2.mol | [Molecular Weight]
411.88 |
| Chemical Properties | Back Directory | [Melting point ]
96-97 °C | [Boiling point ]
608.6±55.0 °C(Predicted) | [density ]
1.214±0.06 g/cm3(Predicted) | [storage temp. ]
Hygroscopic, -20°C Freezer, Under inert atmosphere | [solubility ]
Chloroform (Slightly), Dichloromethane (Slightly) | [form ]
neat | [pka]
13.90±0.46(Predicted) | [color ]
Pale Beige | [Henry's Law Constant]
1.1×104 mol/(m3Pa) at 25℃, HSDB (2015) | [Major Application]
agriculture
environmental | [InChI]
1S/C23H22ClNO4/c1-4-14-28-20-11-6-17(16-21(20)27-3)12-13-25-23(26)22(29-15-5-2)18-7-9-19(24)10-8-18/h1-2,6-11,16,22H,12-15H2,3H3,(H,25,26) | [InChIKey]
KWLVWJPJKJMCSH-UHFFFAOYSA-N | [SMILES]
ClC1=CC=C(C(OCC#C)C(NCCC2=CC=C(OCC#C)C(OC)=C2)=O)C=C1 | [LogP]
4.160 (est) | [EPA Substance Registry System]
Benzeneacetamide, 4-chloro-N-[2-[3-methoxy-4-(2-propyn-1-yloxy)phenyl]ethyl]-.alpha.-(2-propyn-1-yloxy)- (374726-62-2) |
| Hazard Information | Back Directory | [Chemical Properties]
Dicynamid pure product is light yellow powder, melting point 96.4~97.3 ℃, vapor pressure <9.4×10-4mPa(25~50 ℃), distribution coefficient Kow lgP=3.2, Henry's coefficient <9.2×10-5 Pa-m3/mol(25 ℃, calculated value), density(22 ℃)1.24g/L. Solubility in water 4.2mg Solubility in water 4.2mg/L(25℃); Solubility in organic solvents (25℃, g/L): n-hexane 0.042, n-octanol 4.8, toluene 29, methanol 66, ethyl acetate 120, acetone 300, dichloromethane 400 Stable in pH=4~9. | [Uses]
Mandipropamid is a fungicide. It can be used on many fruit and vegetable crops, including potatoes, tomatoes, salad leaves and grapes. Manufactured by Syngenta. | [Definition]
ChEBI: 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide is a monocarboxylic acid amide resulting from the condensation of the carboxy group of p-chloromandelic acid propargyl ether with the amino group of 2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethylamine. It is a monocarboxylic acid amide, a terminal acetylenic compound, an aromatic ether and a member of monochlorobenzenes. | [Production Methods]
The industrial production of mandipropamid begins with the preparation of key intermediates such as 4-chloroacetophenone and vanillin, which undergo condensation and oxidation reactions to form a substituted aromatic ketone. This intermediate is then coupled with a cyclopropyl-containing oxazole derivative through a Friedel–Crafts acylation or similar electrophilic substitution, forming the central methanone bridge. The next step involves constructing the amide bond by reacting the ketone with an amine or ammonia derivative under mild conditions, yielding the final active compound: (RS)-2-(4-chlorophenyl)-N-(cyclopropylmethoxy)-N-(2-methoxyphenyl)acetamide. The synthesis is optimised to avoid protecting groups, simplifying purification and reducing waste. | [Biological Activity]
Mandipropamid (Mandi) is an agrochemical extensively used as fungicide. Mandipropamid specifically induces complex formation between a sixfold mutant of the plant hormone receptor pyrabactin resistance 1 (PYR1) and abscisic acid insensitive (ABI). Mandipropamid is a highly cell permeablelow toxic chemical inducers of proximity in vivo. It induces rapid colocalization of proteins contained fused receptor domain PYRMandi and receiver domain ABI. | [Mechanism of action]
Inhibits spore germination with preventative action. Cellulose synthesis inhibitor. | [storage]
Store at -20°C | [Pesticide Type]
Fungicide |
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| Company Name: |
Merck KGaA
|
| Tel: |
21-20338288 |
| Website: |
www.sigmaaldrich.cn |
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