6627-85-6 Usage
Description
(2-ALLYL-PHENOXY)-ACETIC ACID, also known as 2-allylphenoxyacetic acid, is a chemical compound with the formula C10H11O3. It is a white solid that is soluble in organic solvents and has a molecular weight of 179.19 g/mol. (2-ALLYL-PHENOXY)-ACETIC ACID is commonly used as an intermediate for the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Additionally, it is utilized in the production of polymer resins and adhesives. (2-ALLYL-PHENOXY)-ACETIC ACID is recognized for its potential biological activities, such as anti-inflammatory and analgesic properties. However, it is crucial to handle this compound with care due to its potential to cause irritation to the skin, eyes, and respiratory system.
Uses
Used in Pharmaceutical Industry:
(2-ALLYL-PHENOXY)-ACETIC ACID is used as an intermediate in the synthesis of various pharmaceuticals for its potential biological activities, including anti-inflammatory and analgesic properties. This allows for the development of medications that can help alleviate pain and reduce inflammation.
Used in Agrochemical Industry:
In the agrochemical industry, (2-ALLYL-PHENOXY)-ACETIC ACID serves as an intermediate in the production of various agrochemicals. Its role in this sector is crucial for the development of products that can protect crops and enhance agricultural productivity.
Used in Polymer and Adhesive Production:
(2-ALLYL-PHENOXY)-ACETIC ACID is used in the manufacturing process of polymer resins and adhesives. Its chemical properties make it a valuable component in creating durable and effective bonding agents for various applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6627-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6627-85:
(6*6)+(5*6)+(4*2)+(3*7)+(2*8)+(1*5)=116
116 % 10 = 6
So 6627-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O3/c1-2-5-9-6-3-4-7-10(9)14-8-11(12)13/h2-4,6-7H,1,5,8H2,(H,12,13)
6627-85-6Relevant articles and documents
Photoelectron transfer induced decarboxylation of substituted carboxylic acids across a liquid/liquid interface
Rajesh,Thanulingam,Das, Suresh
, p. 16817 - 16834 (2007/10/03)
Methylene blue photocatalyzed electron transfer reactions of some phenoxyacetic acid derivatives and N-phenylglycine across a liquid/liquid interface led to their efficient decarboxylation. Nanosecond laser flash photolysis studies of this process, in a reverse micellar system of Aerosol- OT (AOT)-benzene-water indicated that the liquid/liquid interface acts as a barrier in controlling the energy wasting back electron transfer. Intramolecular C-C bond forming reactions of these radicals were utilized for the synthesis of various chroman derivatives.
