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Morpholin-4-yl-acetic acid

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Morpholin-4-yl-acetic acid manufacturers

Morpholin-4-yl-acetic acid Basic information
Product Name:Morpholin-4-yl-acetic acid
Synonyms:Carfilzomib Impurity 22;AKOS BBS-00002525;4-MORPHOLINOACETIC ACID;2-(4-MORPHOLINYL)ACETIC ACID;RARECHEM AL BO 0383;TIMTEC-BB SBB010303;Morpholin-4-ylacetic acid Morpholinoacetic acid;4-Morpholine acetic acid
CAS:3235-69-6
MF:C6H11NO3
MW:145.16
EINECS:
Product Categories:Amino Acids and Derivatives
Mol File:3235-69-6.mol
Morpholin-4-yl-acetic acid Structure
Morpholin-4-yl-acetic acid Chemical Properties
Melting point 162-164℃
Boiling point 272℃
density 1.202
Fp 118℃
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka2.25±0.10(Predicted)
color Off-White
InChIInChI=1S/C6H11NO3/c8-6(9)5-7-1-3-10-4-2-7/h1-5H2,(H,8,9)
InChIKeyVIWZVFVJPXTXPA-UHFFFAOYSA-N
SMILESN1(CC(O)=O)CCOCC1
CAS DataBase Reference3235-69-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36
HazardClass IRRITANT
MSDS Information
Morpholin-4-yl-acetic acid Usage And Synthesis
UsesMorpholin-4-yl Acetic Acid was used in preparation of pyrrolidine-fused fullerene multicarboxylates by photoreaction.
DefinitionChEBI: N-(2-Carboxymethyl)-morpholine is an alpha-amino acid.
Synthesis
ETHYL MORPHOLINOACETATE, 98

3235-82-3

MORPHOLIN-4-YL-ACETIC ACID

3235-69-6

b) Synthesis of 2-morpholinoacetic acid Ethyl 2-morpholinoacetate (1 g, 57.8 mmol, 1.0 eq.) was dissolved in 8N HCl and the reaction was stirred at 95°C for 16 hours. Upon completion of the reaction, the reaction mixture was concentrated, quenched, and extracted as in Intermediate Example 15(b). The solvent was removed by distillation to afford the target product 2-morpholinoacetic acid in 96.3% (0.8 g) yield. The product was analyzed by LC-MS (ESI): calculated mass: 145.16; measured mass: 146.3 [M + H]+ (retention time: 0.21 min).

References[1] Patent: WO2013/53983, 2013, A1. Location in patent: Page/Page column 40
[2] Journal of Medicinal Chemistry, 2000, vol. 43, # 8, p. 1489 - 1494
[3] Liebigs Annalen der Chemie, 1983, # 6, p. 950 - 961
[4] Patent: US2015/11548, 2015, A1. Location in patent: Paragraph 0145
[5] Patent: WO2009/48559, 2009, A1. Location in patent: Page/Page column 70
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