7460-95-9 Usage
Molecular structure
A complex chemical compound with a unique structure, consisting of a pentitol (five-carbon sugar alcohol) backbone, an attached amino group, and a cyclohexa-2,4-dien-1-ylidene methyl group.
Pentitol backbone
A five-carbon sugar alcohol that forms the main structure of the compound.
Amino group
A nitrogen-containing functional group attached to the pentitol backbone, contributing to the compound's reactivity and potential interactions with biological systems.
Ketone group
A carbonyl functional group (C=O) within the compound, which may contribute to its reactivity and potential applications in the pharmaceutical and chemical industries.
Z configuration
A specific orientation of the double bond in the cyclohexa-2,4-dien-1-ylidene group, which affects the compound's stereochemistry and interactions with other molecules.
Potential applications
Due to its complex structure and potential interactions with biological systems, 1-deoxy-1-[(Z)-(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]aminopentitol has potential applications in the pharmaceutical and chemical industries.
Further research
More research and testing are required to fully understand the properties and potential uses of this complex compound.
Check Digit Verification of cas no
The CAS Registry Mumber 7460-95-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7460-95:
(6*7)+(5*4)+(4*6)+(3*0)+(2*9)+(1*5)=109
109 % 10 = 9
So 7460-95-9 is a valid CAS Registry Number.
7460-95-9Relevant articles and documents
ELECTRO-ORGANIC REACTIONS. PART 33. REDUCTION OF SUGAR OXIMES
Ryan, Gary,Utley, H. P.,Jones, Haydn F.
, p. 3699 - 3702 (2007/10/02)
Monosaccharide oximes reduce irreversibly at ca.-1.73V vs Ag/AgI in the presence of a proton donor; preparative scale constrant current electro-reduction, in aqueous solution, gives efficient conversion into the corresponding glycamines which are isolated as Schiff base or acetate derivatives.
