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(S)-3-Ethylmorpholine is a morpholine derivative, an organic compound characterized by a six-member ring structure with four carbon atoms, one oxygen atom, and one nitrogen atom. It features an ethyl chain branching off one of the carbon atoms, and the (S)-prefix indicates the presence of stereoisomerism, with the compound existing in at least two non-superimposable mirror image forms. (S)-3-Ethylmorpholine is widely recognized for its role in synthetic organic chemistry.

748117-01-3

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748117-01-3 Usage

Uses

Used in Synthetic Organic Chemistry:
(S)-3-Ethylmorpholine is used as a chemical intermediate for the synthesis of other chemicals. Its unique structure and properties make it a valuable component in the production of various compounds, contributing to the development of new materials and pharmaceuticals.
Used in Pharmaceutical Industry:
(S)-3-Ethylmorpholine is used as a building block in the creation of pharmaceutical compounds. Its versatility in chemical reactions allows for the development of new drugs with potential therapeutic applications, enhancing the range of treatments available for various medical conditions.
Used in Material Science:
(S)-3-Ethylmorpholine is employed as a component in the synthesis of advanced materials, such as polymers and other high-performance materials. Its incorporation into these materials can lead to improved properties, such as increased stability, enhanced reactivity, or altered physical characteristics, which can be beneficial in various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 748117-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,8,1,1 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 748117-01:
(8*7)+(7*4)+(6*8)+(5*1)+(4*1)+(3*7)+(2*0)+(1*1)=163
163 % 10 = 3
So 748117-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO/c1-2-6-5-8-4-3-7-6/h6-7H,2-5H2,1H3/t6-/m0/s1

748117-01-3SDS

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 (3S)-3-ethylmorpholine

1.2 Other means of identification

Product number -
Other names Morpholine,3-ethyl-,(3S)

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:748117-01-3 SDS

748117-01-3Relevant academic research and scientific papers

A concise and efficient synthesis of substituted morpholines

Dugar, Sundeep,Sharma, Amit,Kuila, Bilash,Mahajan, Dinesh,Dwivedi, Sandeep,Tripathi, Vinayak

, (2015/02/19)

A simple and efficient method has been developed for the synthesis of substituted morpholines by a sequence of coupling, cyclization, and reduction reactions of easily available amino alcohols and α-halo acid chlorides. Various mono-, di-, and trisubstituted morpholines, spiro morpholines, and ring-fused morpholines, as well as morpholine homologues, were synthesized in good to excellent yields by a single methodology under similar reaction conditions. The method was also used in a multigram synthesis of (3S)-3-methylmorpholine.

Synthesis of enantiopure 3-substituted morpholines

Bornholdt, Jan,Felding, Jakob,Kristensen, Jesper Langgaard

supporting information; experimental part, p. 7454 - 7457 (2011/01/04)

Enantiopure 3-substituted morpholines were assembled through ring-opening of a N-2-benzothiazolesulfonyl (Bts) activated aziridine with organocuprates followed by a ring annulation reaction with a vinylsulfonium salt under microwave conditions. Deprotecti

2-AMINOBENZOXAZOLE CARBOXAMIDES AS 5HT3 MODULATORS

-

Page/Page column 14; 20, (2008/12/04)

Compounds of formulae I, II and III: are disclosed as 5-HT3 inhibitors. The compounds are useful in treating CINV, IBS-D and other diseases and conditions.

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