4-methylmorpholine-3-carboxylic acid;hydrochloride|1240518-90-4,AngeneChemical

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4-methylmorpholine-3-carboxylic acid;hydrochloride

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Chemical Name:	4-methylmorpholine-3-carboxylic acid;hydrochloride
CAS Number:	1240518-90-4
Product Number:	AG000LGO(AGN-PC-09RRID)
Synonyms:
MDL No:
Molecular Formula:	C6H12ClNO3
Molecular Weight:	181.6174

Identification/Properties
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NMR Spectrum
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Identification/Properties

Computed Properties

Molecular Weight:

181.616g/mol

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

181.051g/mol

Monoisotopic Mass:

181.051g/mol

Topological Polar Surface Area:

49.8A^2

Heavy Atom Count:

Formal Charge:

Complexity:

137

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

N/A

Signal Word:

UN#:

Hazard Statements:

Precautionary Statements:

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

4-Methylmorpholine-3-carboxylic acid hydrochloride, also known as $name$, is a versatile chemical reagent commonly used in chemical synthesis applications. This compound serves as a valuable precursor in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical properties make it an essential building block for the synthesis of complex organic molecules in the laboratory.One of the key applications of $name$ is in the synthesis of peptides and peptide-based drugs. By using $name$ as a starting material, chemists can efficiently introduce specific functional groups and stereochemistry into peptide structures, enabling the creation of novel therapeutic agents with enhanced bioactivity and selectivity. Additionally, $name$ can be utilized in the construction of peptide mimetics and peptidomimetics, which are synthetic compounds designed to mimic the structure and function of natural peptides.Moreover, $name$ finds utility in the development of asymmetric synthesis strategies, where it acts as a chiral auxiliary or ligand in catalytic processes. By incorporating $name$ into the reaction scheme, chemists can promote enantioselective transformations and control the stereochemistry of the final product with high precision. This enables the efficient production of enantiopure compounds with potential applications in the pharmaceutical and agrochemical industries.In summary, 4-Methylmorpholine-3-carboxylic acid hydrochloride plays a crucial role in modern chemical synthesis by facilitating the construction of complex molecules, particularly in the fields of peptide chemistry and asymmetric synthesis. Its versatility and efficacy make it a valuable tool for chemists seeking to explore new synthetic pathways and develop innovative compounds with therapeutic and commercial potential.