1306763-31-4 Usage
Description
(R)-tert-butyl (4-cyano-2,3-dihydro-1H-inden-1-yl)carbamate is an amine derivative characterized by its off-white to white solid appearance. It is a chiral compound, which means it has a non-superimposable mirror image, and is used in various applications due to its unique structural properties.
Uses
Used in Pharmaceutical Industry:
(R)-tert-butyl (4-cyano-2,3-dihydro-1H-inden-1-yl)carbamate is used as a chiral reagent for the synthesis of enantiomerically pure compounds. Its application is crucial in the development of single-enantiomer drugs, which can have significant advantages over racemates in terms of efficacy and safety.
Used in Chemical Synthesis:
(R)-tert-butyl (4-cyano-2,3-dihydro-1H-inden-1-yl)carbamate is used as a building block in the synthesis of various organic compounds, particularly those with chiral centers. Its unique structure allows for the creation of a wide range of molecules with potential applications in different industries.
Used in Research and Development:
In the field of research and development, (R)-tert-butyl (4-cyano-2,3-dihydro-1H-inden-1-yl)carbamate serves as an important compound for studying the effects of chirality on chemical reactions and the properties of molecules. This knowledge can be applied to improve the design and synthesis of new drugs and materials.
Used in Analytical Chemistry:
(R)-tert-butyl (4-cyano-2,3-dihydro-1H-inden-1-yl)carbamate can be employed as a chiral reference standard in analytical chemistry. It helps in the identification and quantification of enantiomers in samples, which is essential for understanding the stereochemistry of biologically active compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1306763-31-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,6,7,6 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1306763-31:
(9*1)+(8*3)+(7*0)+(6*6)+(5*7)+(4*6)+(3*3)+(2*3)+(1*1)=144
144 % 10 = 4
So 1306763-31-4 is a valid CAS Registry Number.
1306763-31-4Relevant articles and documents
IMPROVED PROCESS FOR THE PREPARATION OF OZANIMOD Α-AMINO COMPOUND
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, (2019/04/16)
The present invention relates to an improved process for the preparation of optically chiral amino compound. The present invention particularly relates to the improved process for the preparation of (S)-1-amino-2,3-dihydro-1H-indene-4-carbonitrile, an important intermediate for the synthesis of ozanimod. The present invention more particularly relates to preparation of (S)-1-amino-2,3-dihydro-1H-indene-4- carbonitrile using 4-cyano-1-indanone and α-methylbenzylamine derivatives as starting materials. The present invention specifically relates to preparation of (S)-1- amino-2,3-dihydro-1H-indene-4-carbonitrile comprising diastereoselective chiral amine synthesis by protection with chiral auxiliary ?-methyl benzylamine derivatives followed by reduction and debenzylation.
DEUTERIUM-SUBSTITUTED OXADIAZOLES
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, (2016/10/31)
Described are deuterated modulators of S1P1 receptors, pharmaceutical compositions thereof, and methods of use thereof.
SPHINGOSINE 1 PHOSPHATE RECEPTOR MODULATORS AND METHODS OF CHIRAL SYNTHESIS
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Page/Page column 93, (2011/06/16)
Compounds that selectively modulate the sphingosine 1 phosphate receptor are provided including compounds which modulate subtype 1 of the S1P receptor. Methods of chiral synthesis of such compounds is provided. Uses, methods of treatment or prevention and methods of preparing inventive compositions including inventive compounds are provided in connection with the treatment or prevention of diseases, malconditions, and disorders for which modulation of the sphingosine 1 phosphate receptor is medically indicated.
