22898-01-7 Usage
Description
Sodium 2,2,3,3-tetrafluoropropionate, also known as T292900, is a colorless to pale yellow transparent liquid that serves as a salt form of 2,2,3,3-tetrafluoropropanoic acid. It is characterized by its chemical properties and is utilized in various applications across different industries.
Uses
Used in Agricultural Chemicals:
Sodium 2,2,3,3-tetrafluoropropionate is used as a herbicide in the agricultural industry. It plays a crucial role in methods and formulations designed to prevent the downward migration of agricultural materials, ensuring the effectiveness and targeted application of these substances.
Used in Preventing Downward Migration of Agricultural Materials:
Sodium 2,2,3,3-tetrafluoropropionate is employed as a component in formulations that help prevent the downward migration of agricultural materials. This application is particularly important in maintaining the efficiency and effectiveness of these materials, as it ensures that they remain in the desired location and do not leach into the soil or other unintended areas.
Hazard
Moderately toxic by skin contact. Low tox-
icity by ingestion.
Check Digit Verification of cas no
The CAS Registry Mumber 22898-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,9 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22898-01:
(7*2)+(6*2)+(5*8)+(4*9)+(3*8)+(2*0)+(1*1)=127
127 % 10 = 7
So 22898-01-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H2F4O2.Na/c4-1(5)3(6,7)2(8)9;/h1H,(H,8,9);/q;+1/p-1
22898-01-7Relevant articles and documents
HYDROLYSIS OF FLUOROALKYL-CONTAINING β-AMINOVINYL KETONES
Bazhenova, L. N.,Filyakova, V. I.,Kirichenko, V. E.,Pashkevich, K. I.
, p. 581 - 585 (2007/10/02)
The kinetics of hydrolysis of fluoroalkyl-containing β-aminovinyl ketones R1C(O)CHC(NHR3)R2, in which the substituents CF3 and HCF2CF2 are in the ketone (R1) or enamine parts of the molecule (R2), was studied.In acid (pH 10) media, they hydrolyze with the formation of the corresponding amines and β-diketones.In an alkaline medium, the β-diketones undergo cleavage to fluorinated acids and methyl ketones.The rate constants of hydrolysis in an acid medium change within a range of four orders, depensdng on the nature of the substituents.The presence of a fluoroalkyl group at the enamine reaction center increases the hydrolysis rate.In an alkaline medium, the rate constants vary within one order.