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ChemicalBook--->CAS DataBase List--->1229023-00-0

1229023-00-0

1229023-00-0 Structure

1229023-00-0 Structure
IdentificationBack Directory
[Name]

[2-(4-chloro-2,6-dimethyl-phenyl)-8-methoxy-4-methyl-3 oxo-4,8-diazaspiro[4,5]dec-1-en-1-yl] ethyl carbonate
[CAS]

1229023-00-0
[Synonyms]

spiropidion
[2-(4-chloro-2,6-dimethyl-phenyl)-8-methoxy-4-methyl-3 oxo-4,8-diazaspiro[4,5]dec-1-en-1-yl] ethyl carbonate
Carbonic acid, 3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-yl ethyl ester
[EINECS(EC#)]

815-785-2
[Molecular Formula]

C21H27ClN2O5
[MOL File]

1229023-00-0.mol
[Molecular Weight]

422.9
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS09
[Signal word ]

Warning
[Hazard statements ]

H317-H400-H410-H332
[Precautionary statements ]

P273-P391-P501-P261-P271-P304+P340-P312-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501-P273-P391-P501
Hazard InformationBack Directory
[Uses]

3-(4-Chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-yl Ethyl Carbonate can be useful in national probabilistic risk assessment of newly registered pesticides in agricultural products to propose maximum residue limit (MRL).
[Definition]

ChEBI: Spiropidion is an azaspiro compound that is 1-methoxypiperidine which is fused at position 4 to the 5-position of a 1,5-dihydro-2H-pyrrol-2-one that is substituted at positions 1, 3 and 4 by methyl, 4-chloro-2,6-dimethylphenyl and (ethoxycarbonyl)oxy groups, respectively. It is a proinsecticide developed by Syngenta and used to protect a wide range of crops from some of the most damaging, difficult to control sucking pests such as aphids, whiteflies, Pysllids, armoured scales, soft scales, spider mites, rust mites, and red mites including California red scale, green peach aphid (Myzus persicae), tobacco whitefly etc. It has a role as an EC 6.4.1.2 (acetyl-CoA carboxylase) inhibitor, a proinsecticide and an agrochemical. It is a member of tetramic acids, a member of monochlorobenzenes, an azaspiro compound and a carbonate ester.
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