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Diflubenzuron → Benzoylurea

HRID 1890219
Notes
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Reaction equation

HRID 1890219 reaction equation
[CH:1]1[CH:6]=[C:5](F)[C:4]([C:8]([NH:10][C:11]([NH:13]C2C=C(Cl)C(OC3N=CC(C(F)(F)F)=CC=3Cl)=C(Cl)C=2)=[O:12])=[O:9])=[C:3](F)[CH:2]=1.C1C=C(F)C(C(NC(NC2C=CC(Cl)=CC=2)=O)=O)=C(F)C=1.C1C=C(F)C(C(NC(NC2C=CC(Cl)=C(OC3N=CC(C(F)(F)F)=CC=3Cl)C=2)=O)=O)=C(F)C=1.C1C=C(F)C(C(NC(NC2C=CC(CO/N=C(\C3CC3)/C3C=CC(Cl)=CC=3)=CC=2)=O)=O)=C(F)C=1.C1C=C(F)C(C(NC(NC2C=CC(OC3C=CC(C(F)(F)F)=CC=3Cl)=CC=2F)=O)=O)=C(F)C=1.C1C=C(F)C(C(NC(NC2C=C(Cl)C(OC(F)(F)C(F)F)=C(Cl)C=2)=O)=O)=C(F)C=1.C1C=C(F)C(C(NC(NC2C(Cl)=CC(OC(F)(F)C(F)C(F)(F)F)=C(Cl)C=2)=O)=O)=C(F)C=1.C1C=C(F)C(C(NC(NC2C=CC(OC(F)(F)C(F)OC(F)(F)F)=C(Cl)C=2)=O)=O)=C(F)C=1.C1C=C(F)C(C(NC(NC2C=C(Cl)C(OC(F)(F)C(F)C(F)(F)F)=C(Cl)C=2F)=O)=O)=C(F)C=1.C1C=C(F)C(C(NC(NC2C=C(Cl)C(F)=C(Cl)C=2F)=O)=O)=C(F)C=1.C1C=CC(Cl)=C(C(NC(NC2C=CC(OC(F)(F)F)=CC=2)=O)=O)C=1>>[C:8]([NH:10][C:11]([NH2:13])=[O:12])(=[O:9])[C:4]1[CH:5]=[CH:6][CH:1]=[CH:2][CH:3]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

12

Reactant 11

HCID 37123DiflubenzuronHCID 47445TriflumuronHCID 65651FluazuronHCID 71777LufenuronHCID 91708ChlorfluazuronHCID 91734TeflubenzuronHCID 91741
Hexaflumuron
HCID 91766Flufenoxuron
HCID 93541Novaluron
HCID 6537963(E)-flucycloxuron
HCID 9828359Noviflumuron

Product 1

HCID 69190Benzoylurea

Procedure

chlorfluazuron, bistrifluoron, diflubenzuron, fluazuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron, triflumuron;

Sources & evidence

ORD record
ord-09b346e401ab4782b3eb66d6abc7c591
Source dataset
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08507410B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes