77197-92-3 Usage
Benzene derivative
Cyclopropyl and phenoxy groups attached
1-Cyclopropyl-4-phenoxybenzene is a benzene-based compound with a cyclopropyl group and a phenoxy group attached to its carbon atoms, which modifies its chemical properties.
Pharmaceutical industry use
Synthesis of organic compounds and drug production
1-Cyclopropyl-4-phenoxybenzene is utilized in the pharmaceutical industry for the synthesis of various organic compounds and as a building block in the production of different drugs.
Potential applications
Intermediate in pharmaceutical and agrochemical production
1-Cyclopropyl-4-phenoxybenzene has potential applications as an intermediate in the manufacturing process of various pharmaceuticals and agrochemicals.
Utility in research and industrial processes
Cyclopropyl-substituted benzene derivative
The compound may be useful in academic research and industrial processes that require a cyclopropyl-substituted benzene derivative.
Varying properties and applications
Intended use and specific conditions
The specific properties and applications of 1-Cyclopropyl-4-phenoxybenzene may vary depending on the intended use and the specific conditions under which it is employed.
Check Digit Verification of cas no
The CAS Registry Mumber 77197-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,9 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77197-92:
(7*7)+(6*7)+(5*1)+(4*9)+(3*7)+(2*9)+(1*2)=173
173 % 10 = 3
So 77197-92-3 is a valid CAS Registry Number.
77197-92-3Relevant academic research and scientific papers
BEHAVIOR OF 2- AND 4-CYCLOPROPYLPHENYL ETHERS DURING NITRATION WITH NITRIC ACID IN ACETIC ANHYDRIDE
Mochalov, S. S.,Karpova, V. V.,Shabarov, Yu. S.
, p. 1780 - 1785 (2007/10/02)
During the nitration of 4-cyclopropyl phenyl ethers dilute nitric acid in acetic anhydride formal dealkylation (or dearylation) is realized with substituent entry of the nitro group into the para-substituted phenol which forms.Under analogous conditions the behavior of the corresponding ortho-substituted phenyl ethers depends both on the steric limitations created by the aroxyl (or alkoxyl) fragment and on its polar effect.In the reaction of cyclopropylphenyl ethers with concentrated nitric acid in acetic anhydride the formation of nitrophenols is hardly observed at all.
