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22573-38-2

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22573-38-2 Usage

General Description

(+/-)-3-methyl-1-indanone is a chemical compound with a molecular formula of C10H10O. It is a ketone and belongs to the family of indanone compounds. This chemical is commonly used in the production of fragrances and flavorings due to its pleasant and characteristic odor. It is also utilized in the synthesis of various pharmaceuticals and agrochemicals. Additionally, (+/-)-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. Overall, this chemical compound has a wide range of applications and plays a significant role in the production of various commercial products.

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

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