22573-38-2 Usage
Description
(+/-)-3-methyl-1-indanone, a chemical compound with the molecular formula C10H10O, is a ketone that belongs to the indanone family. (+/-)-3-methyl-1-indanone is known for its pleasant and characteristic odor, making it a valuable component in the production of fragrances and flavorings.
Uses
Used in Fragrance and Flavoring Industry:
(+/-)-3-methyl-1-indanone is used as a key ingredient in the creation of fragrances and flavorings due to its distinctive and appealing scent. Its unique aroma profile contributes to the development of various commercial products, enhancing their sensory appeal.
Used in Pharmaceutical Synthesis:
(+/-)-3-methyl-1-indanone serves as an essential building block in the synthesis of a wide range of pharmaceuticals. Its chemical properties allow it to be incorporated into the structures of various medicinal compounds, contributing to the development of new and effective treatments.
Used in Agrochemical Production:
(+/-)-3-methyl-1-indanone also finds application in the agrochemical industry, where it is utilized in the synthesis of various agrochemicals. Its role in this field is crucial for the development of products that help protect crops and enhance agricultural productivity.
Used in Medicinal Chemistry Research:
(+/-)-3-methyl-1-indanone has been studied for its potential anti-inflammatory and antioxidant properties, making it a subject of interest in the field of medicinal chemistry. Its potential therapeutic effects are being explored for the development of new drugs and treatments for various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 22573-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,7 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22573-38:
(7*2)+(6*2)+(5*5)+(4*7)+(3*3)+(2*3)+(1*8)=102
102 % 10 = 2
So 22573-38-2 is a valid CAS Registry Number.
22573-38-2Relevant articles and documents
Gourley et al.
, p. 1278 (1967)
Preparation of 6α-Substituted Optically Pure Steroid with Thiophene as the A Ring via Assymetric Induction. A Circular Dichroism Study
Macco, Anton A.,Buck, Henk M.
, p. 2655 - 2660 (1981)
A number of assymetrically induced cyclization reactions are described, furnishing specifically substituted steroid-like systems with thiophene as the A ring.Ring closure of achiral compounds give two enantiomeric trans-anti-fused products, containing thr
Exploring the synthetic potential of a marine transaminase including discrimination at a remote stereocentre
Schwarz, Maria,Murphy, Edel J.,Foley, Aoife M.,Woods, David F.,Castilla, Ignacio Abreu,Reen, F. Jerry,Collins, Stuart G.,O'gara, Fergal,Maguire, Anita R.
supporting information, p. 188 - 198 (2021/01/18)
The marine transaminase, P-ω-TA, can be employed for the transamination from 1-aminotetralins and 1-aminoindanes with differentiation of stereochemistry at both the site of reaction and at a remote stereocentre resulting in formation of ketone products with up to 93% ee. While 4-substituents are tolerated on the tetralin core, the presence of 3- or 8-substituents is not tolerated by the transaminase. In general P-ω-TA shows capacity for remote diastereoselectivity, although both the stereoselectivity and efficiency are dependent on the specific substrate structure. Optimum efficiency and selectivity are seen with 4-haloaryl-1-aminotetralins and 3-haloaryl-1-aminoindanes, which may be associated with the marine origin of this enzyme. This journal is
CAGED COMPOUND AND METHOD FOR PRODUCING THE SAME
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Paragraph 0042, (2020/05/20)
PROBLEM TO BE SOLVED: To provide a photoresponsive caged compound that can suppress biological damage and has excellent reaction efficiency, has water solubility, and can perform efficiently spatiotemporal control of bioactive substance such as amino acid
