31638-54-7 Usage
Uses
Used in Pharmaceutical Synthesis:
(1R-endo)-3-amino-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one hydrochloride is used as a key reactant for the synthesis of alpha-amino ketones, which are important intermediates in the production of various pharmaceuticals. These alpha-amino ketones can be further modified to create a wide range of therapeutic agents, including antibiotics, antifungals, and anticancer drugs.
Used in Chemical Research:
In the field of chemical research, (1R-endo)-3-amino-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one hydrochloride serves as a valuable compound for studying the reactivity and selectivity of various synthetic transformations. Its unique structure allows chemists to explore new reaction pathways and develop innovative synthetic strategies for the preparation of complex organic molecules.
Used in Material Science:
(1R-endo)-3-amino-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one hydrochloride may also find applications in material science, where its unique structural features could be exploited to design and synthesize novel materials with specific properties. For example, its incorporation into polymers or other materials could lead to the development of new materials with enhanced mechanical, thermal, or electrical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 31638-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,6,3 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31638-54:
(7*3)+(6*1)+(5*6)+(4*3)+(3*8)+(2*5)+(1*4)=107
107 % 10 = 7
So 31638-54-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H17NO.ClH/c1-9(2)6-4-5-10(9,3)8(12)7(6)11;/h6-7H,4-5,11H2,1-3H3;1H/t6-,7+,10+;/m1./s1
31638-54-7Relevant academic research and scientific papers
Asymmetric reduction of α-keto aldoxime o -ethers
Bosiak, Mariusz J.,Pakulski, Marcin M.
experimental part, p. 316 - 324 (2011/03/18)
The catalytic asymmetric reduction of -keto aldoxime O-methyl, O-benzyl, and O-trityl ethers, derived from substituted acetophenones, with borane/oxazaborolidines, by transfer hydrogenation, and with yeast, was studied. The reduction with borane/oxazaborolidines produced the corresponding -hydroxy oxime ethers, -hydroxy hydroxylamine ethers, and -amino alcohols in 39-78% yields and up to 77% ee. The carbonyl group was selectively reduced by transfer hydrogenation with formic acid-triethylamine catalyzed by RhCl[(R,R)-TsDPEN](Ce, and also with yeast, producing -hydroxy oxime ethers, up to 75% ee and 93% ee, respectively. Georg Thieme Verlag Stuttgart New York.
