288088-57-3

Basic information

• Product Name: 1,2,3-Cyclopentanetriol,4-amino-5-mercapto-,(1R,2R,3R,4S,5R)-(9CI)
• Synonyms: 1,2,3-Cyclopentanetriol,4-amino-5-mercapto-,(1R,2R,3R,4S,5R)-(9CI)
• CAS NO: 288088-57-3
• Molecular Formula: C5H11NO3S
• Molecular Weight: 0
• Product Categories: CYCLOPENTANE
• Mol File: 288088-57-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2,3-Cyclopentanetriol,4-amino-5-mercapto-,(1R,2R,3R,4S,5R)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3-Cyclopentanetriol,4-amino-5-mercapto-,(1R,2R,3R,4S,5R)-(9CI)(288088-57-3)
• EPA Substance Registry System: 1,2,3-Cyclopentanetriol,4-amino-5-mercapto-,(1R,2R,3R,4S,5R)-(9CI)(288088-57-3)

Safety Data

• Hazardous Substances Data: 288088-57-3(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 5 carbon (C), 9 hydrogen (H), 1 nitrogen (N), 2 oxygen (O), and 1 sulfur (S) atoms.

Explanation

The compound belongs to the cyclopentanetriol family, which is a group of organic compounds containing a cyclopentane ring with three hydroxyl (OH) groups.

Explanation

The compound contains an amino group (-NH2) and a mercapto group (-SH), which are important functional groups that contribute to its chemical reactivity and properties.

Explanation

The stereochemistry of a molecule refers to the three-dimensional arrangement of its atoms. In 1,2,3-Cyclopentanetriol,4-amino-5-mercapto-,(1R,2R,3R,4S,5R)-(9CI), the stereochemistry is designated as 1R,2R,3R,4S,5R, which indicates the specific arrangement of the atoms in the molecule.

Explanation

The compound is used in various chemical and pharmaceutical applications, such as a building block in organic synthesis and as a precursor for the synthesis of pharmaceutical products.

Explanation

Due to its stereochemistry and functional groups, the compound is a versatile starting material for the production of complex molecules in the pharmaceutical and chemical industries. This makes it valuable for the development of new drugs and other advanced materials.

Family

Cyclopentanetriol

Functional Groups

Amino and Mercapto

Stereochemistry

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

Applications

Chemical and Pharmaceutical Industries

Versatility

Production of Complex Molecules

Upstream product

• 288088-63-1 C₂₄H₂₈F₃NO₁₀S 
• 170869-79-1 C₂₅H₃₁NO₈S 
• 171031-93-9 C₂₃H₂₉NO₈ 
• 288088-76-6 1D-(1,2,3,4/5)-1,2,3-tri-O-acetyl-4-acetamido-5-acetylthio-1,2,3-cyclopentanetriol 

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