21436-03-3 | (1S,2S)-(+)-1,2-Diaminocyclohexane

Packsize	Purity	Availability	Price	Discounted Price
250mg	99%	in stock	$6.00	$4.00
1g	99%	in stock	$8.00	$5.00
5g	99%	in stock	$15.00	$10.00
10g	99%	in stock	$19.00	$13.00
25g	99%	in stock	$33.00	$23.00

Description

• Catalog Number: AB54693
• Chemical Name: (1S,2S)-(+)-1,2-Diaminocyclohexane
• CAS Number: 21436-03-3
• Molecular Formula: C6H14N2
• Molecular Weight: 114.1888
• MDL Number: MFCD00062986
• SMILES: N[C@H]1CCCC[C@@H]1N

Computed Properties

• Complexity: 62.9
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• XLogP3: -0.3

Upstream Synthesis Route

(1S,2S)-Cyclohexane-1,2-diamine, also known as trans-1,2-Diaminocyclohexane, is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it a valuable building block in the preparation of various organic molecules.In chemical synthesis, (1S,2S)-Cyclohexane-1,2-diamine is utilized as a chiral ligand in asymmetric catalysis. Due to its stereochemistry, it can selectively bind to metal ions and assist in controlling the stereochemistry of the resulting products. This makes it a valuable tool in the production of enantiomerically pure compounds, which are essential in pharmaceuticals, agrochemicals, and fine chemical industries.Additionally, (1S,2S)-Cyclohexane-1,2-diamine can also act as a versatile precursor for the synthesis of complex organic molecules. Its ability to participate in various types of chemical reactions, such as hydrogenation, oxidation, and carbon-carbon bond formation, allows for the efficient construction of intricate structures with high stereocontrol.Overall, (1S,2S)-Cyclohexane-1,2-diamine plays a crucial role in modern chemical synthesis by enabling the creation of diverse and valuable organic compounds with high purity and selectivity.

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