23564-06-9 Usage
Description
THIOPHANAT-ETHYL, a colorless crystalline compound, is a member of the thioureas class. It is specifically the diethyl ester of (1,2-phenylenedicarbamothioyl)biscarbamic acid. This fungicide is known for its effectiveness against a wide range of diseases in various crops, such as fruit, vegetables, turf, and others.
Uses
Used in Agricultural Industry:
THIOPHANAT-ETHYL is used as a fungicide for protecting crops from a broad spectrum of diseases. Its application helps in controlling and preventing issues like eyespot, scab, powdery mildew, and grey mould, ensuring healthier and more productive harvests.
Used in Fruit Crops:
THIOPHANAT-ETHYL is used as a protective agent for fruit crops, safeguarding them from fungal infections that could lead to reduced yield and quality.
Used in Vegetable Crops:
In the vegetable industry, THIOPHANAT-ETHYL is utilized as a fungicide to prevent the growth and spread of harmful fungi, thus maintaining the health and quality of the produce.
Used in Turf and Ornamental Plants:
THIOPHANAT-ETHYL is employed as a fungicidal treatment for turf and ornamental plants, helping to keep them free from diseases and maintaining their visual appeal and overall health.
Used in Other Crops:
Beyond fruit, vegetables, and turf, THIOPHANAT-ETHYL is also used in other types of crops to combat a variety of fungal diseases, ensuring the overall health and productivity of the agricultural sector.
Air & Water Reactions
Hydrolyzed by alkaline media.
Reactivity Profile
THIOPHANAT-ETHYL is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates. This substance is incompatible with copper containing compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 23564-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,6 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23564-06:
(7*2)+(6*3)+(5*5)+(4*6)+(3*4)+(2*0)+(1*6)=99
99 % 10 = 9
So 23564-06-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N4O4S2/c1-3-21-13(19)17-11(23)15-9-7-5-6-8-10(9)16-12(24)18-14(20)22-4-2/h5-8H,3-4H2,1-2H3,(H2,15,17,19,23)(H2,16,18,20,24)
23564-06-9Relevant articles and documents
TMEDA-catalyzed synthesis of N-aryl-N′-ethoxycarbonyl thiourea and arene (or polymethylene)-bis-ethoxycarbonylthiourea derivatives
Lin, Qi,Zhang, You-Ming,Gao, Li-Ming,Wei, Tai-Bao,Wang, Hai
, p. 2051 - 2057 (2007/10/03)
A novel and efficient method for synthesis ethoxycarbonyl isothiocyanate and ethoxycarbonyl thioureas catalyzed by TMEDA is reported. A series of N-aryl-N′-ethoxycarbonyl thioureas and arene (or polymethylene)-bis- ethoxycarbonyl thiourea derivatives have been synthesized in good-to-excellent yields via this method at room temperature.
2-(Pyrazolyloxy) -pyridin-3-ylacetic acid derivatives, agents containing the same and use thereof against noxious fungi and animal parasites
-
, (2008/06/13)
Compounds of the formula I and salts thereof, in which the substituents and the index n have the following meanings: Q is —C(═CHCH3)—COOCH3, —C(═CHOCH3)—COOCH3, —C(═NOCH3)—COOCH3or —C(═NOCH3)—CONH(CH3); R1is hydrogen, halogen, C1-C4-alkyl, C1-C2-haloalkyl, C1-C4-alkoxy or C1-C2-haloalkoxy; R2is halogen, C1-C4-alkyl, C1-C2-haloalkyl, C1-C4-alkoxy; n is 0, 1 or 2, where the substituents R2may be different if n=2; R3is phenyl, pyridyl or pyrimidyl, compositions comprising them and the use of the compounds I and the compositions for controlling harmful fungi and animal pests are described.
Method for combating harmful fungi
-
, (2008/06/13)
A method for control of harmful fungi is provided by treating the fungi, or the materials, plants, the soil or seeds to be protected against fungal infection, with an effective amount of a bisoxime of the formula I or a salt or adduct thereof, the index and the substituents having the following meanings: R1is halogen, alkyl or haloalkyl; R2is cyano, nitro, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, alkylamino, dialkylamino, alkylaminocarbonyl, substituted or unsubstituted phenyl, phenoxy or phenylthio; n is 0, 1, 2 or 3; R3is alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl or phenylalkyl.
