101268-32-0 Usage
Description
(4(3-HYDROXY-3-METHYL-BUTYL)-PHENOXY)-ACETIC ACID, a phenoxyacetic acid derivative with the molecular formula C14H20O4, is a chemical compound that serves as an effective and selective postemergence herbicide. It is instrumental in controlling a range of grassy and broadleaf weeds in agricultural and horticultural settings by disrupting their growth and development, ultimately causing their demise.
Uses
Used in Agricultural and Horticultural Industries:
(4(3-HYDROXY-3-METHYL-BUTYL)-PHENOXY)-ACETIC ACID is used as a postemergence herbicide for controlling a variety of grassy and broadleaf weeds. It is applied to ensure the healthy growth of crops by eliminating unwanted weeds that compete for resources and can potentially reduce crop yields.
It is crucial to handle this chemical with care, as it can be harmful to non-target plants and animals if not used properly. This underscores the importance of adhering to safety guidelines and best practices in its application to minimize environmental impact and protect beneficial flora and fauna.
Check Digit Verification of cas no
The CAS Registry Mumber 101268-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,2,6 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101268-32:
(8*1)+(7*0)+(6*1)+(5*2)+(4*6)+(3*8)+(2*3)+(1*2)=80
80 % 10 = 0
So 101268-32-0 is a valid CAS Registry Number.
101268-32-0Relevant articles and documents
An improved preparation of a tertiary alcohol proline linker and its use in a synthesis of mosquito oostatic hormone
Kochansky,Wagner
, p. 8007 - 8010 (1992)
An improved synthesis of 4-(3'-hydroxy-3'-methylbutyl)phenoxyacetic acid was developed using THF to overcome solubility problems initially encountered in trying to reproduce the published preparation. This hydroxyacid linker was coupled to aminomethyl polystyrene resin and used for a synthesis of the mosquito oostatic hormone by the Fmoc protocol. Attempts to prepare this insect peptide by other techniques had failed because of loss of cyclo-Pro2 from the resin.
