288088-61-9

Basic information

• Product Name: 1,2,3-Cyclopentanetriol,4-amino-5-methoxy-,(1R,2R,3R,4S,5S)-(9CI)
• Synonyms: 1,2,3-Cyclopentanetriol,4-amino-5-methoxy-,(1R,2R,3R,4S,5S)-(9CI)
• CAS NO: 288088-61-9
• Molecular Formula: C6H13NO4
• Molecular Weight: 163.17
• Product Categories: METHOXY
• Mol File: 288088-61-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2,3-Cyclopentanetriol,4-amino-5-methoxy-,(1R,2R,3R,4S,5S)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3-Cyclopentanetriol,4-amino-5-methoxy-,(1R,2R,3R,4S,5S)-(9CI)(288088-61-9)
• EPA Substance Registry System: 1,2,3-Cyclopentanetriol,4-amino-5-methoxy-,(1R,2R,3R,4S,5S)-(9CI)(288088-61-9)

Safety Data

• Hazardous Substances Data: 288088-61-9(Hazardous Substances Data)

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. Cyclopentane Derivative

Explanation

The compound is derived from cyclopentane, a five-membered ring structure with five carbon atoms.
3. Hydroxyl Group

Explanation

A hydroxyl group (-OH) is attached to the cyclopentane ring, which is a functional group consisting of an oxygen atom bonded to a hydrogen atom.
4. Amino Group

Explanation

An amino group (-NH2) is also attached to the cyclopentane ring, which is a functional group consisting of a nitrogen atom bonded to two hydrogen atoms.
5. Methoxy Group

Explanation

A methoxy group (-OCH3) is present at the fourth position of the cyclopentane ring, which is a functional group consisting of an oxygen atom bonded to a methyl group (-CH3).
6. Chiral Molecule

Explanation

The compound is chiral, meaning it has a non-superimposable mirror image. This is due to the specific arrangement of its atoms, which gives it stereochemistry.

Explanation

The stereochemistry of the compound is defined by the (1R,2R,3R,4S,5S) configuration, which describes the spatial arrangement of the atoms in the molecule.
8. Potential Applications
a. Pharmaceuticals

Explanation

Due to its unique structure and properties, the compound may have potential applications in the pharmaceutical industry, possibly as a drug or a precursor to a drug.
b. Organic Synthesis
9. 9CI (Chemical Abstracts Service Registry Number)

Explanation

The 9CI is a unique identifier assigned by the Chemical Abstracts Service (CAS) to the compound, which helps in its identification and classification in scientific databases.

Stereochemistry

(1R,2R,3R,4S,5S)

Upstream product

• 288088-78-8 1L-(1,2,3,5/4)-1,2,3-tri-O-acetyl-5-acetamido-4-O-methyl-1,2,3,4-cyclopentanetetrol 
• 288088-79-9 1L-(1,2,3,4,5/0)-1,2,3-tri-O-acetyl-5-acetamido-4-O-methyl-1,2,3,4-cyclopentanetetrol 
• 288088-73-3 C₁₉H₃₅NO₅Si 
• 288088-74-4 C₂₀H₃₇NO₅Si 
• 171031-90-6 C₂₃H₂₉NO₈ 
• 288088-66-4 C₂₉H₄₃NO₈Si 
• 288088-67-5 C₁₉H₃₅NO₅Si 
• 288088-68-6 C₂₀H₃₇NO₅Si 
• 288088-70-0 C₁₅H₂₅NO₇S 
• 288088-69-7 C₁₄H₂₃NO₅ 
• 288088-71-1 C₁₄H₂₃NO₅ 

Relevant articles and documents

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

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

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