51707-55-2 Usage
Description
5-Phenylcarbamoylamino-1,2,3-thiadiazole is an organic compound with a unique chemical structure that features a thiadiazole ring fused with a phenyl ring and an amide group. 5-Phenylcarbamoylamino-1,2,3-thiadiazole is known for its potential applications in various industries due to its distinct chemical properties.
Uses
Used in Pharmaceutical Industry:
5-Phenylcarbamoylamino-1,2,3-thiadiazole is used as an intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs with specific therapeutic properties.
Used in Chemical Synthesis:
In the field of organic chemistry, 5-Phenylcarbamoylamino-1,2,3-thiadiazole serves as a valuable building block for the creation of more complex molecules. Its reactivity and structural features make it a useful compound in the synthesis of various organic compounds with potential applications in different industries.
Used in Material Science:
5-Phenylcarbamoylamino-1,2,3-thiadiazole's unique chemical structure and properties make it a candidate for the development of new materials with specific characteristics. It can be used in the design and synthesis of advanced materials for various applications, such as electronics, sensors, and coatings.
Used in Agricultural Industry:
5-Phenylcarbamoylamino-1,2,3-thiadiazole can be used as a component in the development of new agrochemicals, such as pesticides or plant growth regulators. Its specific properties may contribute to the enhancement of crop yield and protection against pests.
Used in Research and Development:
Due to its unique structure and potential applications, 5-Phenylcarbamoylamino-1,2,3-thiadiazole is a valuable compound for research and development purposes. It can be used in the study of various chemical reactions and processes, as well as in the development of new methodologies and techniques in organic chemistry.
Trade name
DAZE?; DEFOLIT?; DROPP?;
GINSTAR EC? (thidiazuron + diuron); LEAFLESS?
Tthidiazuron; SN 49537?
Safety Profile
Moderately toxic by
ingestion. Experimental reproductive
effects. When heated to decomposition it
emits toxic fumes of SOx and NOx.
Environmental Fate
Soil. The reported half-life in soil is approximately 26–144 days (Hartley and Kidd,
1987).Photolytic. Rapidly converted to the photoisomer, 1-phenyl-3-(1,2,5-thiadiazol-3-
yl)urea (Worthing and Hance, 1991). When thidiazuron adsorbed by soil was exposed to
UV light (λ <290 nm), 1-phenyl-3-(1,2,5-thiadiazol-3-yl)urea formed as the majo
Check Digit Verification of cas no
The CAS Registry Mumber 51707-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,7,0 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51707-55:
(7*5)+(6*1)+(5*7)+(4*0)+(3*7)+(2*5)+(1*5)=112
112 % 10 = 2
So 51707-55-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N4OS/c14-9(12-8-6-10-13-15-8)11-7-4-2-1-3-5-7/h1-6H,(H2,11,12,14)
51707-55-2Relevant articles and documents
Preparation method 1 - phenyl -3 - (1, 2, 3 - thiadiazol -5 -yl) urea (by machine translation)
-
Paragraph 0024-0033, (2020/10/21)
The 1 -phenyl -3 - (1, 2, 3 -thiadiazol -5 -yl) urea is prepared by reacting 5 amino -1.2.3 - thiadiazole as a raw material, adding a compound solvent, carrying out suction filtration, washing and drying to obtain a pale yellow solid, and obtaining 1 - phenyl -3 - (1, 2 and 3 - thiadiazol -5 -yl) urea. The preparation method has the beneficial effects that the reaction conditions are mild and controllable, the yield is high, the obtained product is high in quality, the solvent boiling point is high, the recovery is convenient, the loss is less, the production cycle is shortened, the solvent recovery utilization rate is all 95% or more, and the product yield is high. (by machine translation)
Plant-protective pesticidal composition
-
, (2008/06/13)
The invention relates to a plant-protective solution containing 2.5 to 40 % by weight of one or more water-insoluble plant-protective ingredient(s) 20 to 71.5 % by weight of dimethylformamide and/or dimethylsulfoxide and/or acetone as water-miscible solvent, 10 to 71.5 % by weight of furfurol and/or furfuryl alcohol as partially water-miscible solvent, 1 to 15 % by weight of commonly used additives such as anionic and/or nonionic surface active agents and macromolecules. The invention also relates to the ready-for-use plant-protective suspension containing 0.2 to 10 % by weight of one or more water-insoluble plant-protective ingredient(s) with a particle size of 0.1 to 50 μm, 0 to 60 % by weight of a fertilizer, 0.2 to 10 % by weight of dimethylformamide and/or dimethylsulfoxide and/or acetone as water-miscible solvent, 0.2 to 10 % by weight of furfurol and/or furfuryl alcohol as partially water-miscible solvent, 0.05 to 2.5 by weight of a commonly used additive such as anionic and/or nonionic surface active agents macromolecules and water in an amount supplementing up to 100 % by weight.
Process for the preparation of 1,2,3-thiadiazol-5-yl ureas
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, (2008/06/13)
A process for the preparation of 1,2,3-thiadiazol-5-yl ureas of the general formula STR1 in which a 1,2,3-thiadiazol-5-carbohydroxam acid derivative of the formula STR2 is dissolved in an inert organic solvent with an acid halide of the formula to form an acylated derivative which then reacts with an amine of the formula STR3 to form the desired product.
