80220-33-3 Usage
Uses
Used in Pharmaceutical Industry:
[(1S,2S)-1-hydroxy-2,3-dihydro-1H-inden-2-yl]acetic acid is used as a synthetic intermediate for the development of various pharmaceuticals. Its hydroxy and carboxylic acid groups facilitate versatile reactions, allowing for the creation of a wide range of drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, [(1S,2S)-1-hydroxy-2,3-dihydro-1H-inden-2-yl]acetic acid is utilized as a building block for the synthesis of novel agrochemicals. Its unique structure and functional groups enable the development of innovative compounds with improved efficacy and selectivity in pest control and crop protection.
Used in Fragrance Industry:
[(1S,2S)-1-hydroxy-2,3-dihydro-1H-inden-2-yl]acetic acid is employed as a key intermediate in the synthesis of complex fragrance molecules. Its indene structure and functional groups contribute to the creation of unique and captivating scents for the perfume and cosmetic industries.
Used in Drug Discovery and Development:
Due to its potential biological activity, [(1S,2S)-1-hydroxy-2,3-dihydro-1H-inden-2-yl]acetic acid is a valuable target for drug discovery and development. Its unique structure and functional groups make it an attractive candidate for the design and synthesis of new therapeutic agents with diverse applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 80220-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,2 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 80220-33:
(7*8)+(6*0)+(5*2)+(4*2)+(3*0)+(2*3)+(1*3)=83
83 % 10 = 3
So 80220-33-3 is a valid CAS Registry Number.
80220-33-3Relevant academic research and scientific papers
The Preparation of Synthetic Analogues of Strigol
Johnson, Alan W.,Gowda, Gopala,Hassanali, Ahmed,Knox, John,Monaco, Sam,et al.
, p. 1734 - 1743 (2007/10/02)
A range of analogues of the natural germination stimulant, strigol, for parasitic weeds of the genera Striga and Orobanche, has been prepared.Most of the products contain an α-formyl-γ-lactone (or α-formyl-γ-lactam) grouping attached through an enol-ether linkage to the 5-position of a but-2-enolide.Some have shown sufficiently high activities as to warrant large-scale field trials.
