3868-12-0 Usage
Chemical structure
1-hydrazinylhexose consists of a hexose molecule (a six-carbon sugar) with a hydrazine functional group attached to it.
Reactivity
The hydrazine group in 1-hydrazinylhexose is highly reactive and can undergo a variety of chemical reactions.
Versatility
1-hydrazinylhexose is a versatile chemical building block used in the synthesis of various pharmaceutical compounds and agrochemicals.
Potential applications
It has potential applications in the field of bioconjugation, targeted drug delivery, and diagnostic imaging in medical applications.
Hexose molecule
A six-carbon sugar that serves as the backbone of the 1-hydrazinylhexose compound.
Hydrazine functional group
A highly reactive chemical group (-NH-NH2) attached to the hexose molecule, responsible for its reactivity and potential applications.
Pharmaceutical synthesis
1-hydrazinylhexose is commonly used as a reactant in the production of diverse organic compounds, including pharmaceutical compounds and agrochemicals.
Bioconjugation
1-hydrazinylhexose can be used to attach drugs or imaging agents to specific biomolecules, enabling targeted drug delivery and diagnostic imaging in medical applications.
Pharmaceutical and biomedical industries
The compound has a wide range of potential uses in these industries, making it a valuable chemical building block.
Check Digit Verification of cas no
The CAS Registry Mumber 3868-12-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,6 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3868-12:
(6*3)+(5*8)+(4*6)+(3*8)+(2*1)+(1*2)=110
110 % 10 = 0
So 3868-12-0 is a valid CAS Registry Number.
3868-12-0Relevant academic research and scientific papers
MAOS of D-gluconic acid, D-glucono-1,4- and 1,5-lactones, esters, hydrazides, and benzimidazoles thereof
El Ashry,Awad,Abdel Hamid,Atta
, p. 329 - 338 (2008/02/12)
Microwave-assisted organic synthesis (MAOS) of D-gluconic acid can be efficiently done by oxidation of D-glucose with bromine water, upon irradiation with microwave (MW). It was also used for the conversion of D-gluconic acid to ethyl D-gluconate, D-glucono-1,4- and 1,5-lactones, gluconyl hydrazide, and gluconyl phenylhydrazide in yields comparable to those obtained by conventional methods, but in much shorter times. A convenient microwave-mediated condensation of D-gluconic acid with o-phenylenediamines provided the respective acyclonucleoside benzimidazole in short time and good yield.
Precursors for the synthesis of substituted 1,3,4-thiadiazole C- nucleosides, analogues of tiazofurin and related compounds
Khorshidi,Rodrigez
, p. 1809 - 1817 (2007/10/02)
The synthesis of 2-substituted 1,3,4-thiadiazole C-glycosides is described by building a heterocyclic system at the aldehyde end of a series of sugar derivatives. Acid catalyzed dehydration of the polyhydroxylic chain resulted in C-nucleoside, an analogue of tiazofurin.
Gluconyl hydrazides
-
, (2008/06/13)
Southern army worm metamorphosis can be interrupted and certain microorganisms, as for example, bacteria, fungi, molds and algae, can be inhibited by contact with an effective growth-inhibiting concentration of gluconic acid hydrazides of the group consisting of the N-(lower alkyl) gluconyl hydrazides.
