3624-30-4 Usage
Description
(6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) is a complex heptane derivative with five hydroxyl groups and two phenylhydrazinylidene groups. (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) has a 6E configuration, which means the two phenylhydrazinylidene groups are positioned on opposite sides of the double bond in the 6th position. Due to limited information available, its properties and potential applications are not well understood.
Uses
Due to the limited information available on (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name), its specific applications are not well defined. However, given its chemical structure, it may have potential uses in various industries such as pharmaceuticals, materials science, or chemical research. It is important to handle this chemical with caution and consult reliable sources for further information on its characteristics and uses.
Check Digit Verification of cas no
The CAS Registry Mumber 3624-30-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,2 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3624-30:
(6*3)+(5*6)+(4*2)+(3*4)+(2*3)+(1*0)=74
74 % 10 = 4
So 3624-30-4 is a valid CAS Registry Number.
3624-30-4Relevant articles and documents
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.