288088-59-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 8 carbon (C), 15 hydrogen (H), 1 nitrogen (N), and 4 oxygen (O) atoms.
2. Cyclic compound
Explanation
The compound has a ring structure, which means the atoms are connected in a closed loop or cycle.
3. Contains three hydroxyl groups
Explanation
Hydroxyl groups (-OH) are functional groups consisting of an oxygen atom bonded to a hydrogen atom. 1,2,3-Cyclopentanetriol,4-amino-5-methoxy-,(1R,2R,3R,4S,5R)-(9CI) has three of these groups attached to its carbon atoms.
4. Contains one amino group
Explanation
An amino group (-NH2) is a functional group consisting of a nitrogen atom bonded to two hydrogen atoms. 1,2,3-Cyclopentanetriol,4-amino-5-methoxy-,(1R,2R,3R,4S,5R)-(9CI) has one amino group attached to one of its carbon atoms.
5. Contains a methoxy substituent
Explanation
A methoxy group (-OCH3) is a functional group consisting of an oxygen atom bonded to a methyl group (-CH3). 1,2,3-Cyclopentanetriol,4-amino-5-methoxy-,(1R,2R,3R,4S,5R)-(9CI) has one methoxy group attached to one of its carbon atoms.
6. Stereochemically defined isomer
Explanation
The compound has a specific spatial arrangement of its atoms, which differentiates it from other isomers with the same molecular formula but different arrangements.
Explanation
This notation describes the absolute configuration of the compound's chiral centers (carbon atoms with four different substituents). The numbers indicate the position of the chiral centers, and the letters (R or S) describe the arrangement of the substituents around each chiral center.
8. Potential for various biological activities
Explanation
Due to its unique structure, 1,2,3-Cyclopentanetriol,4-amino-5-methoxy-,(1R,2R,3R,4S,5R)-(9CI) may have the ability to interact with biological systems, which could lead to potential applications in medicine or pharmaceutical research.
9. Used in pharmaceutical research
Explanation
The compound's unique structure and potential biological activities make it a candidate for further study in the development of new drugs or therapies.
10. Interesting compound for further study and potential applications
Explanation
The compound's unique structure, stereochemistry, and potential biological activities make it a valuable subject for research, which could lead to new discoveries and applications in various fields.
Stereochemistry
(1R,2R,3R,4S,5R)
Check Digit Verification of cas no
The CAS Registry Mumber 288088-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,0,8 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 288088-59:
(8*2)+(7*8)+(6*8)+(5*0)+(4*8)+(3*8)+(2*5)+(1*9)=195
195 % 10 = 5
So 288088-59-5 is a valid CAS Registry Number.
288088-59-5Relevant academic research and scientific papers
Chemical modification of the α-mannosidase inhibitor mannostain A: Synthesis of a potent inhibitor 1L-(1,2,3,5/4)-5-amino-4-O-methyl-1,2,3,4- cyclopentanetetrol
Ogawa, Seiichiro,Morikawa, Takayuki
, p. 4065 - 4072 (2007/10/03)
Demethylthio-, S-demethyl-, and S-ethyl derivatives of the α-mannosidase inhibitor, mannostasin A, were synthesized and evaluated for their inhibition of Jack bean α-mannosidase with the prime objective of elucidating the role of the methylthio group. All
Synthesis of a potent aminocyclitol α-mannosidase inhibitor, 1L-(1,2,3,5/4)-5-amino-4-O-methyl-1,2,3,4-cyclopentanetetrol
Ogawa, Seiichiro,Morikawa, Takayuki
, p. 1047 - 1050 (2007/10/03)
Demethylthio-, de-S-methyl-, and ethylthio-derivatives of the α-mannosidase inhibitor, mannostatin A, have been synthesized and evaluated for their inhibition of Jack bean α-mannosidase in order to elucidate the roles of the methylthio group. All derivati
