| Identification | Back Directory | [Name]
INDOXACARB | [CAS]
173584-44-6 | [Synonyms]
Chebi:38630
INDOXACARB-MP
S-Indoxacarb Solution
indoxacarb (bsi, pa iso, ansi)
S-Indoxacarb@100 μg/ml in Acetone
S-Indoxacarb@1000 μg/mL in Acetone
METHYL 7-CHLORO-2,5-DIHYDRO-2-[N-(METHOXYCARBONYL)-4-(TRIFLUOROMETHOXY)ANILINOCARBONYL]INDENO[1,2-E][1,3,4]OXADIAZINE-4A(3H)CARBOXYLATE
Methyl (S)-7-chloro-2-((methoxycarbonyl)(4-(trifluoromethoxy)phenyl)carbamoyl)-2,5-dihydroindeno[1,2-e][1,3,4]oxadiazine-4a(3H)-carboxylate
Methyl (4as)-7-chloro-2-{(methoxycarbonyl)[4-(trifluoromethoxy)phenyl]carbamoyl}-2,5-dihydroindeno[1,2-E][1,3,4]oxadiazine-4A(3H)-carboxylate
methyl(S)-7-chloro-2,3,4a,5-tetrahydro-2-[methoxycarbonyl(4-trifluoromethoxyphenyl)carbamoyl]indeno[1,2-e][1,3,4]oxadiazine-4a-carboxylate:indoxacarb
Indeno1,2-e1,3,4oxadiazine-4a(3H)-carboxylic acid, 7-chloro-2,5-dihydro-2-(methoxycarbonyl)4-(trifluoromethoxy)phenylaminocarbonyl-, methyl ester, (4aS)- | [EINECS(EC#)]
200-258-5 | [Molecular Formula]
C22H17ClF3N3O7 | [MDL Number]
MFCD03792834 | [MOL File]
173584-44-6.mol | [Molecular Weight]
527.83 |
| Chemical Properties | Back Directory | [Boiling point ]
571.4±60.0 °C(Predicted) | [density ]
1.53±0.1 g/cm3(Predicted) | [storage temp. ]
0-6°C | [solubility ]
Chloroform (Slightly), DMSO (Slightly) | [form ]
Solid | [pka]
-1.75±0.40(Predicted) | [color ]
White to Off-White | [Henry's Law Constant]
1.5×104 mol/(m3Pa) at 25℃, HSDB (2015) | [LogP]
2.209 (est) | [EPA Substance Registry System]
Indoxacarb (173584-44-6) |
| Hazard Information | Back Directory | [Uses]
(S)-Indoxacarb is an enantiomer of Indoxacarb (I654000), a novel oxadiazine insecticide that is bioactivated in lepidopteran larvae. | [Definition]
ChEBI: Indoxacarb is an organochlorine insecticide and a methyl ester. It has a role as a voltage-gated sodium channel blocker. | [Production Methods]
The production of indoxacarb involves a multi-step organic synthesis starting from m-chlorobenzaldehyde, which reacts with malonic acid to form an intermediate compound through a condensation reaction that eliminates water and carbon dioxide. This intermediate, known as SRCA, undergoes hydrogenation reduction in a high-pressure reactor using a catalyst to yield another intermediate, SRCH. The SRCH is then subjected to cyclisation using hydrogen fluoride as a dehydrating agent, forming the final indoxacarb molecule. | [Mechanism of action]
Contact and stomach action. Voltage-dependent sodium channel modulator. | [Pesticide Type]
Insecticide |
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| Company Name: |
Xi'an MC Biotech, Co., Ltd.
|
| Telephone: |
029-89275612 +8618991951683 |
| Website: |
www.chemicalbook.com/ShowSupplierProductsList1759320/0_EN.htm |
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