5395-14-2 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-phenylhydrazinyl)heptose is used as a pharmaceutical compound for its ability to target specific biological pathways. Its unique structure allows it to interact with various biological molecules, making it a promising candidate for the development of new drugs and therapies.
Used in Drug Development:
In the field of drug development, 1-(2-phenylhydrazinyl)heptose is used as a key intermediate in the synthesis of other bioactive molecules. Its chemical properties enable it to be a valuable building block in the creation of novel compounds with potential therapeutic applications.
Used in Organic Chemistry:
1-(2-phenylhydrazinyl)heptose is also used as a building block in organic chemistry. Its seven-carbon monosaccharide structure provides a foundation for the development of new chemical compounds with various applications in different industries, including pharmaceuticals, materials science, and chemical engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 5395-14-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5395-14:
(6*5)+(5*3)+(4*9)+(3*5)+(2*1)+(1*4)=102
102 % 10 = 2
So 5395-14-2 is a valid CAS Registry Number.
5395-14-2Relevant academic research and scientific papers
STUDIES ON AROYL- AND ARYL-HYDRAZIDE DERIVATIVES FROM D-glycero-D-gulo-HEPTANO-1,4-LACTONE
Sharaf, Saber M.,Sallam, Mohammed A. E.,Shenawy, Hamdy A. El
, p. 39 - 48 (2007/10/02)
A series of aroyl- and aryl-hydrazide derivatives was prepared from D-glycero-D-gulo-heptono-1,4-lactone (1). the reactivity of the NH proton in these hydrazides, in terms of their dissociation constants (pKa), was determined from their electronic spectra, and correlated to the Hammett ? values of the substituents.Comparable reactivities of the NH protons for the compounds, and the effect of the substituent, were studied by n.m.r. spectroscopy.Decomposition of the aroylhydrazides with copper(II) sulfate or nitrous acid resulted in the regeneration of 1.
