ChemicalBook--->CAS DataBase List--->113158-40-0

113158-40-0

113158-40-0 Structure

113158-40-0 Structure
IdentificationBack Directory
[Name]

Fenoxaprop-P
[CAS]

113158-40-0
[Synonyms]

fenoxyprop
FENOXAPROP-P
(R)-FENOXAPROP-P
(r)-propanoicaci
Fenoxaprop-p-ehtyl
FENOXAPROP-P (R-ENANTIOMER)
FENOXAPROP-P PESTANAL, 100 MG
fenoxaprop-p (bsi,draft e-iso,draft f-iso)
(2R)-2-[4-(6-Chloro-2-benzoxazolyloxy)phenoxy]propionic acid
(r)-2-(4-((6-chloro-2-benzoxazolyl)oxy)phenoxy)propanoicacid
(2R)-2-[4-(6-Chlorobenzoxazole-2-yloxy)phenoxy]propionic acid
(R)-2-[4-[(6-Chlorobenzoxazol-2-yl)oxy]phenoxy]propionic acid
(R)-2-[4-(6-chloro-1,3-benzoxazol-2-yloxy)phenoxy]propionic ...
(R)-2-[4-(6-Chloro-1,3-benzoxazol-2-yloxy)phenoxy]propionic acid
Propanoic acid, 2-[4-[(6-chloro-2-benzoxazolyl)oxy]phenoxy]-, (2R)-
[Molecular Formula]

C16H12ClNO5
[MDL Number]

MFCD01311798
[MOL File]

113158-40-0.mol
[Molecular Weight]

333.72
Chemical PropertiesBack Directory
[Melting point ]

158 °C
[Boiling point ]

506.8±58.0 °C(Predicted)
[density ]

1.425±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[form ]

neat
[pka]

3.16±0.10(Predicted)
[Major Application]

agriculture
environmental
[InChI]

1S/C16H12ClNO5/c1-9(15(19)20)21-11-3-5-12(6-4-11)22-16-18-13-7-2-10(17)8-14(13)23-16/h2-9H,1H3,(H,19,20)/t9-/m1/s1
[InChIKey]

MPPOHAUSNPTFAJ-SECBINFHSA-N
[EPA Substance Registry System]

Propanoic acid, 2-[4-[(6-chloro-2-benzoxazolyl)oxy]phenoxy]-, (2R)- (113158-40-0)
Safety DataBack Directory
[Hazard Codes ]

N
[Risk Statements ]

50/53
[Safety Statements ]

60-61
[WGK Germany ]

2
[RTECS ]

UA2452300
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Aquatic Acute 1
Aquatic Chronic 1
Repr. 2
Skin Sens. 1
STOT RE 2
Hazard InformationBack Directory
[Uses]

Fenoxaprop-P is an agro-product, used in pesticide formulations.
[Production Methods]

Fenoxaprop-P is commercially produced through a multi-step synthesis involving chlorinated benzoxazole intermediates. Production typically begins with the preparation of mercapto-6-chlorobenzoxazole and 2,6-dichlorobenzoxazole, which are key intermediates. These compounds undergo etherification and esterification reactions to form the active ingredient fenoxaprop-P-ethyl.
[Mechanism of action]

Unclear but thought to kill weeds by disrupting lipid metabolism
[Pesticide Type]

Metabolite; Herbicide
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