68044-69-9 Usage
Uses
Used in Organic Synthesis:
(6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) is used as a key intermediate in organic synthesis for the creation of various complex organic compounds. Its unique structure and functional groups facilitate multiple chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Research:
In the field of chemical research, (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) serves as a model compound for studying the reactivity and properties of heptane derivatives with multiple functional groups. Researchers use (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) to explore new reaction pathways, develop innovative synthetic methods, and gain insights into the behavior of similar complex molecules.
Used in Pharmaceutical Development:
(6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) is employed as a starting material or a building block in the development of new pharmaceuticals. Its structural diversity and the presence of multiple reactive sites make it a promising candidate for the design and synthesis of novel drug molecules with potential therapeutic applications.
Used in Material Science:
In material science, (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) is used as a component in the development of advanced materials with specific properties. Its unique structure and functional groups can be exploited to create materials with tailored characteristics, such as improved mechanical strength, thermal stability, or chemical resistance, for various industrial applications.
Used in Analytical Chemistry:
(6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) is utilized as a reference compound or a standard in analytical chemistry for the calibration of instruments and the development of new analytical methods. Its well-defined structure and properties make it an ideal candidate for validating the performance of analytical techniques and ensuring the accuracy of experimental results.
Check Digit Verification of cas no
The CAS Registry Mumber 68044-69-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,4 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68044-69:
(7*6)+(6*8)+(5*0)+(4*4)+(3*4)+(2*6)+(1*9)=139
139 % 10 = 9
So 68044-69-9 is a valid CAS Registry Number.
68044-69-9Relevant academic research and scientific papers
STRUCTURE AND ANOMERIC CONFIGURATION OF THE 3,6-ANHYDRO-OSAZONE DERIVATIVES OBTAINED FROM D-altro-2-HEPTULOSE PHENYLOSAZONE
Sallam, Mohammed A. E.
, p. 139 - 148 (2007/10/02)
Dehydration of D-altro-2-heptulose phenylosazone with methanolic sulfuric acid afforded two 3,6-anhydro-osazone derivatives (2 and 3).Compound 3 was obtained as the preponderant isomer, with inversion at C-1 (C-3 of the starting osazone), and 2 was obtained without inversion.Refluxing of 3 with copper sulfate afforded the C-nucleoside analog, namely, 2-phenyl-4-β-D-ribofuranosyl-1,2,3-osotriazole (4).Acetylation of 4 afforded the tri-O-acetyl derivative 5.The anomeric configuration was determined by c.d. and n.m.r. spectroscopy.The mass spectra of compounds 2-5 are discussed.
