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Morpholin-3-yl-acetic acid ethyl ester hydrochloride, with the molecular formula C8H16ClNO3, is a hydrochloride salt of ethyl 3-morpholin-4-ylpropanoate. It is a chemical compound that serves as an intermediate in organic synthesis, characterized by its improved stability and solubility due to its hydrochloride salt form.

761460-01-9

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761460-01-9 Usage

Uses

Used in Pharmaceutical Industry:
Morpholin-3-yl-acetic acid ethyl ester hydrochloride is utilized as a building block in the synthesis of various pharmaceutical compounds. Its role in drug development is crucial, as it contributes to the creation of medications that address a range of health conditions.
Used as a Reagent in Organic Chemical Reactions:
In addition to its applications in the pharmaceutical sector, Morpholin-3-yl-acetic acid ethyl ester hydrochloride also functions as a reagent in organic chemical reactions. This versatility allows it to be employed across different areas of chemical research and development, facilitating the synthesis of a variety of organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 761460-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,1,4,6 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 761460-01:
(8*7)+(7*6)+(6*1)+(5*4)+(4*6)+(3*0)+(2*0)+(1*1)=149
149 % 10 = 9
So 761460-01-9 is a valid CAS Registry Number.

761460-01-9SDS

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 Ethyl 3-morpholinylacetate

1.2 Other means of identification

Product number -
Other names Ethyl 2-(morpholin-3-yl)acetate hydrochloride

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:761460-01-9 SDS

761460-01-9Upstream product

761460-01-9Downstream Products

761460-01-9Relevant academic research and scientific papers

Process for producing enantiopure beta-amino acid derivatives, and enantiopure beta-amino acid derivatives

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, (2008/06/13)

Process for producing enantiopure β-amino acid derivatives corresponding to general formula (I) R1-NZ-CHR2—CH2—COOR3 (I) in which R1 and R2 independently denote organic residues optionally forming a cyclic substituent, R3 denotes H or an organic residue, and Z represents H or an amino function-protecting group, comprising a step in which a mixture of enantiomers of a compound corresponding to general formula (II) R1-NZ-CHR2—CH2—COOR4 (II) in which R1, R2 and Z are as defined for formula (I), and R4 is an organic residue, is subjected to hydrolysis in the presence of a lipase.

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