(S)-(4-Methylmorpholin-3-yl)methanol

Name: (S)-(4-Methylmorpholin-3-yl)methanol
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CAS No. 1620510-50-0
Cat. No. CS-0061776
Purity≥97%
MDL No.MFCD26792482

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(S)-(4-Methylmorpholin-3-yl)methanol|CS-0061776

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General Information

CAS No. 1620510-50-0
Cat. No. CS-0061776
Purity ≥97%
MDL No. MFCD26792482
Storage RT, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₆H₁₃NO₂
Molecular Weight 131.17
Synonym(s) [(3S)-4-Methyl-3-morpholinyl]methanol
SMILES CN1CCOC[C@@H]1CO

Description

(S)-4-Methylmorpholin-3-ylmethanol is a chiral building block featuring a hydroxymethyl-functionalized morpholine ring. This configuration enables stereoselective transformations in medicinal chemistry, particularly in the synthesis of kinase inhibitors and bioactive heterocycles. The pendant hydroxyl group facilitates further derivatization through etherification or esterification under standard conditions.

Application

(S)-4-Methylmorpholin-3-ylmethanol serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to morpholine-based scaffolds. Its bench-stable hydroxymethyl group facilitates straightforward derivatization, while the stereogenic center supports enantioselective synthesis. The molecule exhibits excellent functional group tolerance and compatibility with standard coupling and protection protocols, making it ideal for iterative library construction and API development.

Safety Information

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GHS Pictogram :	GHS No : GHS05
Signal Word : Danger	UN#: 1760
Class : 8	Packing Group : Ⅲ
Hazard Statements : H314
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501

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Computational Chemistry Data

TPSA 32.7
LogP -0.6907
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 1

Other Classifications

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Building Blocks Skeleton Aliphatic heterocycle compounds Morpholine compounds

Key Words

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(S)-(4-Methylmorpholin-3-yl)methanol

CAS No. 1620510-50-0

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