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3235-69-6

3235-69-6 Structure

3235-69-6 Structure
IdentificationMore
[Name]

MORPHOLIN-4-YL-ACETIC ACID
[CAS]

3235-69-6
[Synonyms]

2-(4-MORPHOLINYL)ACETIC ACID
4-MORPHOLINOACETIC ACID
AKOS BBS-00002525
MORPHOLIN-4-YL-ACETIC ACID
MORPHOLINOACETIC ACID
RARECHEM AL BO 0383
TIMTEC-BB SBB010303
4-Morpholine acetic acid
4-Morpholineacetic acid
Morpholin-4-ylacetic acid Morpholinoacetic acid
[Molecular Formula]

C6H11NO3
[MDL Number]

MFCD00504633
[Molecular Weight]

145.16
[MOL File]

3235-69-6.mol
Chemical PropertiesBack Directory
[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
[pka]

2.25±0.10(Predicted)
[color ]

Off-White
[InChI]

InChI=1S/C6H11NO3/c8-6(9)5-7-1-3-10-4-2-7/h1-5H2,(H,8,9)
[InChIKey]

VIWZVFVJPXTXPA-UHFFFAOYSA-N
[SMILES]

N1(CC(O)=O)CCOCC1
[CAS DataBase Reference]

3235-69-6(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Exclamation Mark (GHS07)Environment (GHS09)
GHS02,GHS07,GHS09
[Signal word ]

Warning
[Hazard statements ]

H228-H250-H260-H315-H319-H335-H410
[Precautionary statements ]

P403-P501c
[Hazard Codes ]

Xi
[Risk Statements ]

36
[HazardClass ]

IRRITANT
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethyl acetate-->Sulfuric acid-->Tetrahydrofuran-->Sodium sulfate-->Sodium chloride-->Sodium bicarbonate-->Morpholine-->tert-Butyl bromoacetate-->Ethyl morpholinoacetate, 98-->Methyl N-morpholinoacetate
[Preparation Products]

Ethyl morpholinoacetate, 98-->4-Morpholineacetyl chloride
Hazard InformationBack Directory
[Uses]

Morpholin-?4-?yl Acetic Acid was used in preparation of pyrrolidine-fused fullerene multicarboxylates by photoreaction.
[Definition]

ChEBI: 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
Spectrum DetailBack Directory
[Spectrum Detail]

MORPHOLIN-4-YL-ACETIC ACID(3235-69-6)1HNMR
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