6627-85-6 Usage
General 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. It is also used in the production of polymer resins and adhesives. (2-ALLYL-PHENOXY)-ACETIC ACID is known for its potential biological activities including anti-inflammatory and analgesic properties. It is important to handle this compound with care as it has the potential to cause irritation to the skin, eyes, and respiratory system.
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.
