Florpyrauxifen

HCID 67420724CAS 943832-81-3

Basic information

Standard SMILES
COc1c(Cl)ccc(-c2nc(C(=O)O)c(Cl)c(N)c2F)c1F
InChIKey
XFZUQTKDBCOXPP-UHFFFAOYSA-N
Molecular formula
C13H8Cl2F2N2O3
Average molar mass
349.11 g/mol
Monoisotopic mass
347.98800392

Overview

Florpyrauxifen is a pyridinemonocarboxylic acid that is picolinic acid which is substituted at positions 3, 4, 5, and 6 by chlorine, amino, fluorine, and 4-chloro-2-fluoro-3-methoxyphenyl groups, respectively. An auxin herbicide developed by Dow AgroSciences and sold as the corresponding benzyl ester, florpyrauxifen-benzyl. It has a role as a herbicide and a synthetic auxin. It is a pyridinemonocarboxylic acid, an aromatic ether, an aminopyridine, a biaryl, a member of monochlorobenzenes and a member of monofluorobenzenes.

Names & identifiers

Preferred name
Florpyrauxifen
IUPAC
4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylic acid
English name
florpyrauxifen
Molecular formula
C13H8Cl2F2N2O3
Molecular weight
349.12

Names & synonyms

FlorpyrauxifenFlorpyrauxifen [ISO]7SE2CM4FZV4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylic acidflorpyrauxifene4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropicolinic acid4-Amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoro-2-pyridinecarboxylic acid2-Pyridinecarboxylic acid, 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoro-CHEBI:133650DTXSID50873862XDE-848XR-848
Show more names
Degarelix Impurity 8Florpyrauxifen (>85%)Florpyrauxifen in MethanolArylex Impurity 3 (Florpyrauxifen)Florpyrauxifen2-Pyridinecarboxylic acid, 4-amino-3-chloro-6-(4-chloro-2fluoro-3-methoxyphenyl)-5-fluoro-
RefChem:140764DTXCID301012065878-990-6943832-81-3UNII-7SE2CM4FZVSCHEMBL2471056SCHEMBL29370743SCHEMBL29390242

Database identifiers

CAS
943832-81-3
PubChem CID
67420724
DTXSID
DTXSID50873862
ChEBI
CHEBI:133650
UNII
7SE2CM4FZV
EC Number
878-990-6
Nikkaji
J3.617.442K

Properties

Computed structural properties

XLogP
3.1
Topological polar surface area
85.4 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
7
Rotatable bonds
3
Heavy atoms
22

Physicochemical properties

Boiling point
488.5 · 488.5±45.0 °C(Predicted)
Density
1.593 · 1.593±0.06 g/cm3(Predicted)
pka
3.14 · 3.14±0.34(Predicted)
Henry's Law Constant
3.2 · 3.2×107 mol/(m3Pa) at 25℃, Ebert et al. (2023)
FDA UNII
7 SE2CM4FZV · 7SE2CM4FZV
Symbol(GHS)
7 · GHS07,GHS09

Safety & regulation

GHS classification

GHS Classification · 4 items

Warning

H317 (100%): May cause an allergic skin reaction [Warning Sensitization, Skin]

P261, P272, P273, P280, P302+P352, P321, P333+P317, P362+P364, P391, and P501 (click each P-code to see the statement)

The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Hazard information

Regulatory InformationRegulation (EC) No 1107/2009 (amended)
Hazard Classes and CategoriesSkin Sens. 1 (100%)

Safety data

Signal word
Warning
Symbol(GHS)
GHS07,GHS09
Hazard statements
H410-H400-H317
Precautionary statements
P273-P391-P501-P273-P391-P501-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501

Chemistry & industry

Applications

UsesFlorpyrauxifen is a part of the preparation for post-emergence florpyrauxife-benzyl herbicides.

Suppliers21 total

陕西科贝莱药物研发有限公司13119135307 · [email protected]
艾吉析科技(上海)有限公司17717235263 · [email protected]
江苏智芯廷科技有限公司18221391031 · [email protected]
成都蓝蜻蜓生物技术有限公司028-87856149; 15208320722 · [email protected]
南通菡芳生物科技有限公司[email protected] 18017580634 · [email protected]
Additional notes · 1 item

DefinitionChEBI: Florpyrauxifen is a pyridinemonocarboxylic acid that is picolinic acid which is substituted at positions 3, 4, 5, and 6 by chlorine, amino, fluorine, and 4-chloro-2-fluoro-3-methoxyphenyl groups, respectively. An auxin herbicide developed by Dow AgroSciences and sold as the corresponding benzyl ester, florpyrauxifen-benzyl. It has a role as a herbicide and a synthetic auxin. It is a pyridinemonocarboxylic acid, an aminopyridine, a biaryl, a member of monochlorobenzenes, a member of monofluorobenzenes and an aromatic ether.

Related reactions

5 records

Linked notes

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