91390-34-0 Usage
General Description
2,4,5-trichlorophenyl (2-fluoroethyl)carbamate is a chemical compound consisting of a trichlorophenyl group and a 2-fluoroethylcarbamate group. It is commonly used as a pesticide and insecticide due to its ability to effectively control a wide range of pests and insects. However, it has been banned or restricted in many countries due to its harmful effects on human health and the environment. The chemical is known to be toxic to both humans and animals, and exposure can lead to symptoms such as nausea, vomiting, and dizziness. Additionally, it has been found to have negative impacts on aquatic life and ecosystems. As a result, its use is heavily regulated, and alternatives are being sought for more sustainable pest control methods.
Check Digit Verification of cas no
The CAS Registry Mumber 91390-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,9 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91390-34:
(7*9)+(6*1)+(5*3)+(4*9)+(3*0)+(2*3)+(1*4)=130
130 % 10 = 0
So 91390-34-0 is a valid CAS Registry Number.
91390-34-0Relevant articles and documents
Studies on Synthesis and Anticancer Activity of Selected N-(2-Fluoroethyl)-N-nitrosoureas
Johnston, Thomas P.,Kussner, Conrad L.,Carter, Ronald L.,Frye, Jerry L.,Lomax, Nancita R.,et al.
, p. 1422 - 1426 (2007/10/02)
An activated carbamate, 2-nitrophenyl (2-fluoroethyl)nitrosocarbamate (3), was used to advantage in the synthesis of the water-soluble (2-fluoroethyl)nitrosoureas 6a-d from 2-aminoethanol, (1α,2β,3α)-2-amino-1,3-cyclohexanediol, cis-2-hydroxycyclohexanol, and 2-amino-2-deoxy-D-glucose.In a variation of this method, 2,4,5-trichlorophenyl (2-fluoroethyl)carbamate (4) was used to prepare the urea from which the essentially water-insoluble N'-(2,6-dioxo-3-piperidinyl)-N-(2-fluoroethyl)-N-nitrosourea (6e) was derived.The anticancer activity of these nitrosoureas was determined against the murine tumors B16 melanoma and Lewis lung carcinoma and found to be significant and comparable to their chloroethyl counterparts.On the basis of results from both systems, the dihydroxycyclohexyl derivative 6b may be the most effective.