63076-61-9 Usage
Uses
Used in Pharmaceutical Industry:
2,4-dichloro-1-(pentyloxy)benzene is used as a chemical intermediate for the production of pharmaceuticals. It serves as a key component in the synthesis of certain drugs, contributing to the development of new medications and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-dichloro-1-(pentyloxy)benzene is utilized as an intermediate in the manufacturing process of agrochemicals. Its role in the synthesis of these compounds aids in the creation of products designed to protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
2,4-dichloro-1-(pentyloxy)benzene is employed as a building block in the synthesis of other organic compounds. Its versatile chemical structure allows it to be a valuable precursor in the preparation of a range of organic molecules for various applications.
Safety Considerations:
It is crucial to handle 2,4-dichloro-1-(pentyloxy)benzene with caution due to its toxic properties. It poses a risk if swallowed, inhaled, or comes into contact with the skin, and may cause skin and eye irritation. To ensure safety, it is imperative to follow proper safety procedures, including the use of appropriate protective equipment and working in a well-ventilated area.
Check Digit Verification of cas no
The CAS Registry Mumber 63076-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,7 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63076-61:
(7*6)+(6*3)+(5*0)+(4*7)+(3*6)+(2*6)+(1*1)=119
119 % 10 = 9
So 63076-61-9 is a valid CAS Registry Number.
63076-61-9Relevant academic research and scientific papers
Monochlorination of n-Alkyl Phenyl Ethers in Micellar Sodium Dodecyl Sulfate
Jaeger, David A.,Wyatt, Jacqueline R.,Robertson, Raymond E.
, p. 1467 - 1470 (2007/10/02)
The effect of chain length on the regioselectivity and rate of monochlorination of C6H5OR (1: a = n-C5H11; b, R = n-C9H19; c, R = n-C12H25) with Cl2 in micellar sodium dodecyl sulfate was determined.On going from 1a to 1b to 1c, only modest changes were observed in the para/ortho product ratio and in relative rate.These results were interpreted to indicate that the hydrophilic character of C6H5O dominates the lipophilic character of R in the micellar reactivity of the ethers.
