trans-4-Morpholinocyclohexanol hydrochloride


Chemical Name: trans-4-Morpholinocyclohexanol hydrochloride
CAS Number: 1588441-09-1
Product Number: AG001QXX(AGN-PC-0WAN5D)
Synonyms:
MDL No:
Molecular Formula: C10H20ClNO2
Molecular Weight: 221.7243

Identification/Properties


Computed Properties
Molecular Weight:
221.725g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
221.118g/mol
Monoisotopic Mass:
221.118g/mol
Topological Polar Surface Area:
32.7A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
149
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



Trans-4-Morpholinocyclohexanol hydrochloride is a versatile compound commonly used in chemical synthesis for the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and properties make it a valuable reagent in various synthetic processes.One key application of trans-4-Morpholinocyclohexanol hydrochloride is in the asymmetric synthesis of chiral compounds. As a chiral auxiliary, this compound can impart stereochemical control in reactions, allowing for the selective formation of enantiomerically pure products. This is particularly important in the pharmaceutical industry, where the chirality of a compound can significantly impact its biological activity and pharmacokinetic properties.Additionally, trans-4-Morpholinocyclohexanol hydrochloride is used as a building block in the synthesis of complex molecules. Its hydroxyl and amino functional groups make it a valuable starting material for the construction of more elaborate chemical structures through various chemical transformations such as nucleophilic substitutions, acylations, and reductions.Overall, trans-4-Morpholinocyclohexanol hydrochloride plays a crucial role in enabling chemists to access diverse chemical structures and develop new synthetic methodologies for the efficient production of important compounds in the fields of pharmaceuticals, agrochemicals, and beyond.