438051-03-7 Usage
Description
(1S,2S)-N-BOC-1-AMINO-2-INDANOL is a chemical compound with the molecular formula C14H21NO3. It is a derivative of indanol, a bicyclic aromatic compound, and features a BOC (tert-butyloxycarbonyl) protecting group. (1S,2S)-N-BOC-1-AMINO-2-INDANOL is often used as a chiral building block in the synthesis of pharmaceuticals and other organic compounds due to its (1S,2S) stereochemistry and unique aromatic and steric properties.
Uses
Used in Pharmaceutical Industry:
(1S,2S)-N-BOC-1-AMINO-2-INDANOL is used as a chiral building block for the synthesis of various pharmaceuticals. Its unique stereochemistry and indanol structure make it a valuable component in the development of new drugs with specific biological activities.
Used in Organic Synthesis:
(1S,2S)-N-BOC-1-AMINO-2-INDANOL is used as a chiral intermediate in the synthesis of other organic compounds. Its BOC protecting group allows for selective reactions to occur, making it a versatile compound in organic chemistry.
Used in Research and Development:
(1S,2S)-N-BOC-1-AMINO-2-INDANOL is used in research and development for studying the effects of stereochemistry on the biological activities of compounds. Its different enantiomers can have distinct properties, making it an important tool for understanding the relationship between molecular structure and biological function.
Check Digit Verification of cas no
The CAS Registry Mumber 438051-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,0,5 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 438051-03:
(8*4)+(7*3)+(6*8)+(5*0)+(4*5)+(3*1)+(2*0)+(1*3)=127
127 % 10 = 7
So 438051-03-7 is a valid CAS Registry Number.
438051-03-7Relevant articles and documents
3-(5-HYDROXY-1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE DERIVATIVES AND USES THEREOF
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Paragraph 1910-1911, (2020/02/05)
The present disclosure provides a compound of Formula (I′): or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, wherein Rx, X1, X2, and R1 are as defined herein, and methods of making and using same.
Expeditious assembly of a 2-Amino-4H-chromene skeleton by using an enantioselective Mannich intramolecular ring cyclization-tautomerization cascade sequence
Ren, Qiao,Siau, Woon-Yew,Du, Zhiyun,Zhang, Kun,Wang, Jian
supporting information; experimental part, p. 7781 - 7785 (2011/08/08)
Easy to assemble! An enantioselective cascade Mannich intramolecular ring cyclization-tautomerization reaction of malononitrile with 2-hydroxyl N-protected α-amido sulfone is described (see scheme), which provides a new route to the synthesis of the privi
Enantioselective synthesis of densely functionalized pyranochromenes via an unpredictable cascade Michael-oxa-Michael-tautomerization sequence
Ren, Qiao,Gao, Yaojun,Wang, Jian
supporting information; experimental part, p. 13594 - 13598 (2011/02/26)
A surprising example of enantioselective cascade Michael-oxa-Michael- tautomerization reactions of malononitrile and benzylidenechromanones has been developed. In this case, malononitrile functions as both nucleophile and electrophile. Meanwhile, a simple
