17768-63-7 Usage
Uses
Used in Pharmaceutical Applications:
2-(benzylamino)-3,4,5,6,7-pentahydroxyheptanenitrile (non-preferred name) is used as a pharmaceutical intermediate for its potential role in the synthesis of bioactive compounds. Its unique structure, including the benzylamino and pentahydroxyheptane moieties, may contribute to the development of new drugs with specific therapeutic effects.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(benzylamino)-3,4,5,6,7-pentahydroxyheptanenitrile (non-preferred name) serves as a key building block for the creation of more complex organic molecules. Its versatile functional groups allow for various chemical reactions, facilitating the synthesis of a wide range of organic compounds for different applications.
Used in Chemical Research:
2-(benzylamino)-3,4,5,6,7-pentahydroxyheptanenitrile (non-preferred name) is utilized in chemical research to explore its reactivity, stability, and potential interactions with other molecules. Understanding its properties can lead to insights into new chemical reactions or the discovery of novel applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 17768-63-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,6 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17768-63:
(7*1)+(6*7)+(5*7)+(4*6)+(3*8)+(2*6)+(1*3)=147
147 % 10 = 7
So 17768-63-7 is a valid CAS Registry Number.
17768-63-7Relevant academic research and scientific papers
LIMITATIONS OF THE AMINONITRILE SYNTHESIS. NEW PRODUCTS FROM D-GLUCOSE, D-GALACTOSE, AND D-MANNOSE
Albarran, Juan C. Palacios,Galan, Emilio Roman,Perez, Juan A. Galbis
, p. 117 - 128 (2007/10/02)
The reaction of aldoses with an excess of amine and hydrogen cyanide can yield a series of cyclic and acyclic compounds in addition to the expected α-aminoaldononitriles.The nature of these unexpected products depends on the specific reaction conditions a
