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Parathion → Profenofos

HRID 1252272
Notes
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Reaction equation

HRID 1252272 reaction equation
C[O:2][P:3]([O:7][C:8]1[CH:9]=[C:10](Cl)[C:11]([Br:15])=[CH:12][C:13]=1[Cl:14])([O:5][CH3:6])=[S:4].COP(O[C:24]1[CH:29]=CC([N+]([O-])=O)=C[CH:25]=1)(OC)=S.[CH3:33]COP(OC1C=CC([N+]([O-])=O)=CC=1)(OCC)=S.COP(OC1C=CC([N+]([O-])=O)=C(Cl)C=1)(OC)=S.CC1C=C(OP(OC)(OC)=S)C=CC=1[N+]([O-])=O.COP(OC1C=C(Cl)C(Cl)=CC=1Cl)(OC)=S.CC1C=C(OP(OC)(OC)=S)C=CC=1SC.COP(OC1C=CC(C#N)=CC=1)(OC)=S.CCOP(OC1C=CC(Cl)=CC=1Cl)(OCC)=S.CCOP(O)(N(C(C)C)C1C=CC(SC)=C(C)C=1)=O.CCOP(SC1C=CC=CC=1)(CC)=S.COP(OC1C=CC(SC2C=CC(OP(OC)(OC)=S)=CC=2)=CC=1)(OC)=S.CCCSP(OC1C=CC(Cl)=CC=1Cl)(OCC)=S.CCOP(OC1C=CC=CC=1C(OC(C)C)=O)(NC(C)C)=S.CCOP(OC1C=CC(S(C)=O)=CC=1)(OCC)=S>>[CH3:25][CH2:24][CH2:29][S:2][P:3]([O:7][C:8]1[CH:9]=[CH:10][C:11]([Br:15])=[CH:12][C:13]=1[Cl:14])([O:5][CH2:6][CH3:33])=[O:4]
ParticipantsProcedureSources & evidenceReaction notes

Participants

16

Reactant 15

HCID 991ParathionHCID 3346FenthionHCID 4130Methyl ParathionHCID 5392TemephosHCID 7328DichlofenthionHCID 8292FensulfothionHCID 9298Fenchlorphos
HCID 10372
Chlorthion
HCID 13676Fonofos
HCID 16422Bromophos
HCID 17522Cyanophos
HCID 31200Fenitrothion
HCID 32872Isofenphos
HCID 36870Prothiofos
HCID 44586308ethoxy-N-(3-methyl-4-methylsulfanylphenyl)-N-propan-2-ylphosphonamidic acid

Product 1

HCID 38779Profenofos

Procedure

trifenophos; bromophos; mercaptoprophos; methylparathion; parathion; chlorthion; fenitrothion; fenchlorphos; fenthion; cyanophos; dichlofenthion; fenamiphos; fonofos; jodfenfos; temephos; prothiophos; isofenphos; fensulfothion and lepthophos.

Sources & evidence

ORD record
ord-0d5306d687fa4a69aa4837c0d6ceff25
Source dataset
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04742056

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes