70995-08-3 Usage
Description
Phenol, 4-nitro-2-phenoxy-, also known as Folpet, is a chemical compound that serves as a fungicide and pesticide. It is used to protect crops from fungal diseases and is applied on fruits, vegetables, and ornamental plants. Phenol, 4-nitro-2-phenoxyworks by inhibiting the growth of fungi and preventing their spread.
Uses
Used in Agriculture:
Phenol, 4-nitro-2-phenoxyis used as a fungicide and pesticide for protecting crops from various fungal diseases. It is applied on fruits, vegetables, and ornamental plants to inhibit the growth of fungi and prevent their spread.
As a Hazardous Substance:
Phenol, 4-nitro-2-phenoxyis classified as a hazardous substance and should be handled and disposed of with care to prevent harm to humans, animals, and the environment. Proper safety measures and guidelines should be followed during its use to minimize potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 70995-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,9 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70995-08:
(7*7)+(6*0)+(5*9)+(4*9)+(3*5)+(2*0)+(1*8)=153
153 % 10 = 3
So 70995-08-3 is a valid CAS Registry Number.
70995-08-3Relevant articles and documents
The Smiles Rearrangement of 2-Aryloxy-5-nitrophenoxides. Attempted Routes to Benzoxirens and Tribenzotrioxonins
Ramsden, Christopher A.
, p. 2456 - 2463 (2007/10/02)
Formation of dibenzo-p-dioxins by the pyrolysis of 2-halogenophenoxides does not appear to involve intermediate benzoxirens.Thermal self-condensation to potassium 2-bromo-5-nitrophenoxide (1b) gave a mixture of 2,7- and 2,8-dinitrobenzo-p-dioxins (6d) and (6e).The mechanism of formation of the 2,8-isomer (6e) is shown to involve Smiles rearrangement of potassium 2-(2-bromo-5-nitrophenoxy)-5-nitrophenoxide (9a).Further examples of Smiles rearrangements of 2-aryloxy-5-nitrophenoxides and an attempted synthesis of the tribenzotrioxonin derivatives (16) are described.
