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61213-25-0

61213-25-0 Structure

61213-25-0 Structure
IdentificationMore
[Name]

Fluorochloridone
[CAS]

61213-25-0
[Synonyms]

3-chloro-4-(chloromethyl)-1-[3-(trifluoromethyl)phenyl]pyrrolidin-2-one
FLUORCHLORIDONE
FLUOROCHLORIDON
FLUOROCHLORIDONE
FLUROCHLORIDON
FLUROCHLORIDONE
RACER
1-(m-trifluoromethylphenyl)-3-chloro-4-chloromethyl-2-pyrrolidone
3-chloro-4-(chloromethyl)-1-(3-(trifluoromethyl)phenyl)-2-pyrrolidinon
3-chloro-4-(chloromethyl)-1-(3-(trifluoromethyl)phenyl)-2-pyrrolidinone
r40244
(3RS,4RS,3RS,4RS)-3-chloro-4-chloromethyl-1-α,α,α-trifluoro-m-tolyl-2-pyrrolidone(3:1)
3-chloro-4-(chloromethyl)-1-(3-(trifluoromethyl)phenyl)-2-pyrrolidione
FLUROCHLORIDON (MIXTURE OF ISOMERS),PEST
flurochloridone (bsi,draft e-iso,draft f-iso)
raiser
(3RS, 4RS
(3RS,4RS
3RS,4RS)-3-chloro-4-chloromethyl-1-(α,α,α-trifluoro-m-tolyl)-2-pyrrolidone(3:1)
1-[3-(Trifluoromethyl)phenyl]-3-chloro-4-(chloromethyl)pyrrolidin-2-one
[EINECS(EC#)]

262-661-3
[Molecular Formula]

C6H10ClFO6
[MDL Number]

MFCD00144317
[Molecular Weight]

232.59
[MOL File]

61213-25-0.mol
Chemical PropertiesBack Directory
[Melting point ]

67.65°C
[Boiling point ]

212.5 °C
[density ]

1.3924 (estimate)
[Fp ]

>100 °C
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

-3.59±0.60(Predicted)
[color ]

Pale Brown to Light Brown
[Henry's Law Constant]

2.6×102 mol/(m3Pa) at 25℃, Duchowicz et al. (2020)
[LogP]

3.360
[CAS DataBase Reference]

61213-25-0(CAS DataBase Reference)
[NIST Chemistry Reference]

2-Pyrrolidinone, 3-chloro-4-(chloromethyl)-1-[3-(trifluoromethyl)phenyl]-(61213-25-0)
[EPA Substance Registry System]

61213-25-0(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S27:Take off immediately all contaminated clothing .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RTECS ]

UY5746500
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Allyl chloride-->Allyl bromide-->3-Aminobenzotrifluoride-->Dichloroacetyl chloride-->Dichloroacetamide-->N-Allyl-2,2-dichloro-N-[3-(trifluoromethyl)phenyl]acetamide-->2,2'-Bipyridine-->Copper(I) chloride-->1,2-Dichloroethane
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Fluorochloridone(61213-25-0).msds
Hazard InformationBack Directory
[Description]

Flurochloridone is a pre-emergence herbicide used to control a range of weeds in umbelliferous crops and other such as cereals and potatoes. It has a moderate aqueous solubility and is not considered volatile. Under certain conditions it can be persistent in soils but tends not to be in water-sediment systems. Data for human health suggests a low mammalian oral toxicity but there may be risks for reproduction/development and fluorochloridone is classified as a skin sensitiser. With the exception of algae where toxicity is high, toxicity is moderate for most species.
[Chemical Properties]

Brown solid. Easily soluble in acetone, chlorobenzene, ethanol, xylene and other organic solvents, with a solubility of 100-150g/L. Solubility in kerosene <5g/L. The solubility in water is 28mg/L. Partition coefficient (n-octanol/water) 2300 (20°C). The half-life is 7d at 60°C and pH 4, 18d at 60°C and pH 7, and the half-life in soil is 11-100d.
[Uses]

Flurochloridon can be used in herbicidal composition to control weed in crop fields.
[Definition]

ChEBI: Flurochloridone is a member of pyrrolidines, a member of (trifluoromethyl)benzenes and an organochlorine compound. It has a role as a carotenoid biosynthesis inhibitor, an agrochemical and a herbicide.
[Synthesis]

The synthesis of Fluorochloridone is as follows:To a 1L three-neck flask, N-allyl-N-dichloroacetyl-m-trifluoromethylaniline (31.1 g, 0.1 mol) and 715 ml of 1,2-dichloroethane were added as a solvent, dissolved under stirring, and then added. Cuprous chloride (2.97g, 0.03mol) and 2,2-bipyridyl (4.68g, 0.03mol) were reacted at 80°C for 3 hours, cooled to room temperature, and the reaction solution was filtered through a short silica gel column to give dichloromethane. Elution and desolvation yielded 31.3 g of pyrotropone, a content of 97%, an anti-contrast ratio of ≥3:1, and a yield of 97.6%.61213-25-0.png
[Metabolic pathway]

From hydrolytic and photolytic studies of flurochloridone in buffer solution, no hydrolysis of flurochloridone occurs at pH 5, 7, or 9 at 25°C or at pH 5 at 40°C. Appreciable hydrolysis occurs at 40°C at pH 7 and 9 with half-lives of 190 and 140 days, respectively. Five hydrolytic degradation products and six photolytic degradation products are identified. The major photolytic degradation product which contains 39% of the radioactivity is 4-(chloromethyl)-3-hydroxy-1-[3- (trifluoromethyl)phenyl]-2-pyrrolidinone with a mixture of cis and trans isomers. The formation of this major degradation product suggests that the major photolytic pathway involves homolytic cleavage of the carbon ? chlorine bond at the 3-position of the pyrrolidinone ring and the free radical intermediate can react with water to give the major product or eliminate the hydrogen radical to form 4- (chloromethyl)-1,5-dihydro-1-[3- (trifluoromethyl)phenyl]pyrrol-2H-one.
[Mode of action]

Flurochloridone is the active substance of some pre-emergence herbicides. It has an inhibitory effect on the synthesis of carotenoids, which protect chlorophylls against oxidative stress.
[Toxicity evaluation]

The acute oral LD50 of male rats is 4000 mg/kg, the acute transdermal LD50 of rabbits is >5000 mg/kg, and the acute inhalation of rats is LC50 10.3 mg/L (4h). Slightly irritating to rabbit skin and eyes.
[References]

[1] Patent: CN107868029, 2018, A. Location in patent: Paragraph 0012-0018
[Pesticide Type]

Herbicide
Spectrum DetailBack Directory
[Spectrum Detail]

Fluorochloridone(61213-25-0)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

61213-25-0(sigmaaldrich)
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