79200-57-0 | (1R,2S,3R,5R)-3-Amino-5-(hydroxymethyl)cyclopentane-1,2-diol hydrochloride

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$29.00	$21.00
250mg	95%	in stock	$57.00	$40.00
500mg	95%	in stock	$96.00	$68.00
1g	95%	in stock	$157.00	$110.00
5g	95%	in stock	$550.00	$385.00
10g	95%	in stock	$1,025.00	$717.00
25g	95%	in stock	$2,550.00	$1,785.00

Description

• Catalog Number: AB48325
• Chemical Name: (1R,2S,3R,5R)-3-Amino-5-(hydroxymethyl)cyclopentane-1,2-diol hydrochloride
• CAS Number: 79200-57-0
• Molecular Formula: C6H14ClNO3
• Molecular Weight: 183.6333
• MDL Number: MFCD06799068
• SMILES: OC[C@H]1C[C@H]([C@@H]([C@@H]1O)O)N.Cl

Computed Properties

• Complexity: 120
• Covalently-Bonded Unit Count: 2
• Defined Atom Stereocenter Count: 4
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 5
• Rotatable Bond Count: 1

Upstream Synthesis Route

The compound (1R,2S,3R,5R)-3-Amino-5-(hydroxymethyl)cyclopentane-1,2-diol hydrochloride is a valuable tool in chemical synthesis due to its versatile chemical reactivity and unique structural features. It serves as a chiral building block with multiple reactive sites, allowing it to participate in a variety of synthetic transformations. In chemical synthesis, this compound can be used as a key intermediate in the preparation of complex molecules with specific stereochemical configurations. Its amino and hydroxymethyl groups enable it to engage in a range of reactions such as nucleophilic substitution, acylation, and condensation reactions, leading to the formation of diverse chemical bonds and functional groups. Additionally, the cyclopentane ring structure of this compound imparts rigidity and spatial constraints, which can be advantageous for controlling the stereochemistry of the final products. By incorporating (1R,2S,3R,5R)-3-Amino-5-(hydroxymethyl)cyclopentane-1,2-diol hydrochloride into a synthetic scheme, chemists can access new pathways for the efficient construction of complex molecules with desired stereochemical outcomes.