741288-31-3

Basic information

• Product Name: 3-Morpholinecarboxylicacid,methylester,(3S)-(9CI)
• Synonyms: 3-Morpholinecarboxylicacid,methylester,(3S)-(9CI);(S)-Methyl Morpholine-3-carboxylate;3-Morpholinecarboxylic acid, Methyl ester, (3S)-;Methyl (S)-3-Morpholinecarboxylate;Methyl (3S)-3-Morpholinecarboxylate hydrochloride (1:1);(3S)-3-Morpholinecarboxylic acid methyl ester;(S)-3-Morpholinecarboxylic acid methyl ester HCl;methyl(S)-morpholine-3-carboxylate
• CAS NO: 741288-31-3
• Molecular Formula: C₆H₁₁NO₃
• Molecular Weight: 145.16
• Product Categories: CARBOXYLICESTER
• Mol File: 741288-31-3.mol

Chemical Properties

• Boiling Point: 202.2±30.0 °C(Predicted)
• Appearance: /
• Density: 1.106±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
• PKA: 6.96±0.40(Predicted)
• CAS DataBase Reference: 3-Morpholinecarboxylicacid,methylester,(3S)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Morpholinecarboxylicacid,methylester,(3S)-(9CI)(741288-31-3)
• EPA Substance Registry System: 3-Morpholinecarboxylicacid,methylester,(3S)-(9CI)(741288-31-3)

Safety Data

• Hazardous Substances Data: 741288-31-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3-Morpholinecarboxylic acid, methyl ester, (3S)-(9CI) is used as a building block for the production of various pharmaceuticals. Its unique chemical structure and reactivity enable the synthesis of a wide range of therapeutic agents, contributing to the development of new and improved medications.
Used in Fine Chemicals Industry:
In the fine chemicals industry, 3-Morpholinecarboxylic acid, methyl ester, (3S)-(9CI) serves as an essential intermediate for the synthesis of specialty chemicals. Its versatile properties allow for the creation of high-value compounds used in various applications, such as fragrances, dyes, and other specialty products.
Used in Agrochemical Industry:
3-Morpholinecarboxylic acid, methyl ester, (3S)-(9CI) is utilized as an intermediate in the manufacturing of agrochemicals. Its role in the synthesis of various agrochemicals helps address the needs of the agricultural sector, contributing to the development of effective and sustainable solutions for crop protection and enhancement.
Used as a Solvent in Chemical Reactions:
3-Morpholinecarboxylic acid, methyl ester, (3S)-(9CI) also functions as a solvent in various chemical reactions. Its ability to dissolve a wide range of substances and facilitate reaction processes makes it a valuable component in the synthesis of numerous compounds across different industries.
Used in Medicinal Chemistry and Drug Development:
Due to its diverse chemical reactivity and biological properties, 3-Morpholinecarboxylic acid, methyl ester, (3S)-(9CI) has potential applications in the field of medicinal chemistry and drug development. It serves as a promising candidate for the discovery and optimization of new therapeutic agents, driving innovation in the pharmaceutical and healthcare sectors.

Upstream product

• 1096365-35-3 (S)-methyl 4-(2-(trimethylsilyl)ethylsulfonyl)morpholine-3-carboxylate 

Downstream Products

• 1065333-05-2 (3S)-4-(4-(5-methyl-2-phenyloxazol-4-ylmethoxy)benzyl)morpholine-3-carboxylic acid 
• 1065333-40-5 (3S)-4-(4-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)benzyl)morpholine-3-carboxylic acid 
• 1065333-06-3 (3S)-4-(4-(5-methyl-2-phenyloxazol-4-ylmethoxy)benzyl)morpholine-3-carboxylic acid methyl ester 
• 1065333-41-6 (3S)-4-(4-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)benzyl)morpholine-3-carboxylic acid methyl ester 

Relevant articles and documents

Bromoethylsulfonium salt-a more effective annulation agent for the synthesis of 6- and 7-membered 1,4-heterocyclic compounds

(Chemical Equation Presented) Reaction of bromoethylsulfonium salt with 1,2-/1,3-aminoalcohols gave six- and seven-membered rings in good-to-excellent yields. The reactions proceed through generation of a vinyl sulfonium salt followed by annulation to give 1,4-heterocyclic compounds such as morpholines and benzoxazepines in a simple procedure. The method accommodates a range of nitrogen substituents and the amino alcohol can be substituted by amino thiols and diamines to give thiomorpholines, piperazines and benzodiazepines.