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CAS

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1052209-96-7

(5S)-5-Phenyl-3-morpholinone, also known as EMDO or N-phenylmorpholin-3-one, is a white crystalline powder with a molecular formula of C11H11NO2. It is soluble in organic solvents but insoluble in water. This chemical compound is recognized for its potential applications in various fields, including pharmaceuticals, agrochemicals, and dyes, due to its unique properties and reactivity.

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  • 1052209-96-7 Structure

  • Basic information

    1. Product Name: (5S)-5-Phenyl-3-morpholinone
    2. Synonyms: (5S)-5-Phenyl-3-morpholinone;(S)-5-Phenylmorpholin-3-one;(5S)-5-Phenylmorpholin-3-one
    3. CAS NO:1052209-96-7
    4. Molecular Formula: C10H11NO2
    5. Molecular Weight: 177
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1052209-96-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.149
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: (5S)-5-Phenyl-3-morpholinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5S)-5-Phenyl-3-morpholinone(1052209-96-7)
    11. EPA Substance Registry System: (5S)-5-Phenyl-3-morpholinone(1052209-96-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1052209-96-7(Hazardous Substances Data)

1052209-96-7 Usage

Uses

Used in Pharmaceutical Synthesis:
(5S)-5-Phenyl-3-morpholinone is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic benefits. Its chemical structure allows for versatile reactions that can lead to the creation of a variety of medicinal compounds.
Used in Agrochemical Production:
In the agrochemical industry, (5S)-5-Phenyl-3-morpholinone is utilized as a key intermediate in the production of various agrochemicals, contributing to the development of effective solutions for pest control and crop protection.
Used in Dye Manufacturing:
(5S)-5-Phenyl-3-morpholinone is employed in the manufacturing of dyes, where its chemical properties are leveraged to produce a range of colorants for different applications, including textiles and other industrial uses.
Used in Neurological Disorder Treatment Research:
(5S)-5-Phenyl-3-morpholinone is used as a subject of research for its potential role in the treatment of neurological disorders, given its unique chemical structure that may interact with biological systems in ways that could alleviate symptoms or treat the underlying conditions.
Used in Cancer Treatment Research:
(5S)-5-Phenyl-3-morpholinone is also under investigation for its potential use in cancer treatment, where it may contribute to the development of novel therapeutic agents that target cancer cells while minimizing harm to healthy cells.
Used in Pain Management Drug Development:
Owing to its mild sedative and analgesic effects, (5S)-5-Phenyl-3-morpholinone is used in the development of new drugs for pain management, offering a potential alternative or adjunct to existing analgesics.
It is crucial to handle (5S)-5-Phenyl-3-morpholinone with care due to its potential toxic effects if ingested or inhaled in large amounts, emphasizing the need for proper safety measures during its use in research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1052209-96-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,2,2,0 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1052209-96:
(9*1)+(8*0)+(7*5)+(6*2)+(5*2)+(4*0)+(3*9)+(2*9)+(1*6)=117
117 % 10 = 7
So 1052209-96-7 is a valid CAS Registry Number.

1052209-96-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (5S)-5-Phenylmorpholin-3-one

1.2 Other means of identification

Product number -
Other names (S)-5-oxo-piperazine-2-carboxylic acid methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1052209-96-7 SDS

1052209-96-7Relevant articles and documents

SUBSTITUTED MORPHOLINE DERIVATIVES AS ROR GAMMA MODULATORS

-

, (2018/07/29)

The present disclosure is directed to compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein ring A, R1, R2, R3, X1, X2, m and n are as defined herein, which are active as modulators of retinoid-related orphan receptor gamma t (RORyt). These compounds prevent, inhibit, or suppress the action of RORyt and are therefore useful in the treatment of RORyt mediated diseases, disorders, syndromes or conditions such as, e.g., pain, inflammation, COPD, asthma, rheumatoid arthritis, colitis, multiple sclerosis, psoriasis, neurodegenerative diseases and cancer. (I)

Aminoheteroaryl benzamides as kinase inhibitors

-

, (2016/02/15)

The present invention provides a compound of Formula (I) or a salt thereof; and therapeutic uses of these compounds. The present invention further provides pharmaceutical compositions comprising these compounds, and compositions comprising these compounds with a therapeutic co-agent.

TRICYCLIC MODULATORS OF TNF SIGNALING

-

, (2016/11/02)

The invention provides tricyclic heterocyclic compounds, pharmaceutically acceptable salts, prodrugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variables are defined herein. The compounds of the invention may be useful for treating immunological and oncological conditions.

Diastereoselective synthesis of novel 5-substituted morpholine-3-phosphonic acids: Further exploitation of N-acyliminium intermediates

Bonilla-Landa, Israel,Viveros-Ceballos, José Luis,Ordó?ez, Mario

, p. 485 - 487 (2014/05/06)

The first diastereoselective total synthesis of 5-substituted morpholine-3-phosphonic acids is reported. The principal feature of the synthesis is the introduction of a dimethyl phosphonate group into 5-substituted morpholin-3-ones. The procedure is based

Amine-promoted asymmetric (4+2) annulations for the enantioselective synthesis of tetrahydropyridines: A traceless and recoverable auxiliary strategy

Hu, Pengfei,Hu, Jian,Jiao, Jiajun,Tong, Xiaofeng

, p. 5319 - 5322 (2013/06/05)

Gone, without a trace: The in situ reaction of 2-(acetoxymethyl)buta-2,3- dienoate and a secondary amine produces a 2-methylene-3-oxobutanoate equivalent that can be used in asymmetric [4+2] annulations with N-tosylimines to provide tetrahydropyridines in

4-(1,3-Thiazol-2-yl)morpholine derivatives as inhibitors of phosphoinositide 3-kinase

Alexander, Rikki,Balasundaram, Ahrani,Batchelor, Mark,Brookings, Daniel,Crepy, Karen,Crabbe, Tom,Deltent, Marie-France,Driessens, Frank,Gill, Andrew,Harris, Sue,Hutchinson, Gillian,Kulisa, Claire,Merriman, Mark,Mistry, Prakash,Parton, Ted,Turner, James,Whitcombe, Ian,Wright, Sara

scheme or table, p. 4316 - 4320 (2009/04/06)

4-(1,3-Thiazol-2-yl)morpholine derivatives have been identified as potent and selective inhibitors of phosphoinositide 3-kinase. The SAR data of selected examples are presented and the in vivo profiling of compound 18 is shown to demonstrate the utility of this class of compounds in xenograft models of tumor growth.

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