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Serine, 3-ethoxy-O-ethyl-, ethyl ester is a chemical compound derived from serine, an essential amino acid crucial for protein synthesis in the body. This ethyl ester derivative serves as a key building block in the synthesis of various pharmaceutical compounds, such as antiviral and anticancer drugs. It is characterized by its clear, colorless liquid form, a slightly sweet odor, and solubility in water and most organic solvents. Due to its potential health hazards, Serine, 3-ethoxy-O-ethyl-, ethyl ester should be handled and used with caution, and is primarily utilized in research and industrial applications.

61040-21-9

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61040-21-9 Usage

Uses

Used in Pharmaceutical Industry:
Serine, 3-ethoxy-O-ethyl-, ethyl ester is used as a building block for the synthesis of pharmaceutical compounds, specifically for the development of antiviral and anticancer drugs. Its unique structure allows it to be a valuable component in creating effective medications targeting a range of diseases.
Used in Flavor and Fragrance Industry:
In addition to its pharmaceutical applications, Serine, 3-ethoxy-O-ethyl-, ethyl ester is also utilized in the production of certain flavors and fragrances. Its slightly sweet odor makes it a suitable candidate for use in the creation of various scent profiles and taste enhancements.
Used in Research Applications:
Serine, 3-ethoxy-O-ethyl-, ethyl ester plays a significant role in research settings, where it is employed to study the properties and potential uses of serine and its derivatives. This helps scientists and researchers to better understand the compound's behavior and its interactions with other molecules, leading to advancements in both medicine and other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 61040-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,4 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61040-21:
(7*6)+(6*1)+(5*0)+(4*4)+(3*0)+(2*2)+(1*1)=69
69 % 10 = 9
So 61040-21-9 is a valid CAS Registry Number.

61040-21-9SDS

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 (2S)-2-amino-3,3-diethoxypropanoate

1.2 Other means of identification

Product number -
Other names -

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:61040-21-9 SDS

61040-21-9Relevant academic research and scientific papers

CONSTRAINED COMPOUNDS AS CGRP-RECEPTOR ANTAGONISTS

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Page/Page column 110-111, (2008/06/13)

The invention encompasses constrained bicyclic and tricyclic CGRP-receptor antagonists, methods for identifying them, pharmaceutical compositions comprising them, and methods for their use in therapy for treatment of migraine and other headaches, neurogenic vasodilation, neurogenic inflammation, thermal injury, circulatory shock, flushing associated with menopause, airway inflammatory diseases, such as asthma and chronic obstructive pulmonary disease (COPD), and other conditions the treatment of which can be effected by the antagonism of CGRP-receptors.

Ethyl α-amino-β,β-diethoxypropionate, a useful synthon for the preparation of 3,4-fused pyridine-6-carboxylates from aromatic aldehydes

Singh, Sunil K.,Dekhane, Mouloud,Le Hyaric, Mireille,Potier, Pierre,Dodd, Robert H.

, p. 379 - 391 (2007/10/03)

An efficient synthesis of ethyl α-amino-β,β-diethoxypropionate (1), via a titanium tetrachloride-catalyzed coupling reaction of ethyl nitroacetate and triethyl orthoformate, is described. Condensation of 1 with various aldehydes followed by reduction and

Synthesis of serine analogues to be used as modified phospho acceptor sites in substrates of protein kinase C

Broxterman, H. J. G.,Liskamp, R. M. J.

, p. 46 - 52 (2007/10/02)

Serine and threonine analogues (compounds 2-6) are readily accessible by reaction of the anion of N,N-dibenzylglycine ethyl ester (1) with an appropriate carbonyl compound.These analogues will be incorporated into Protein Kinase C (PKC) substrates.The serine aldehyde derivative 7 was used for the preparation of the corresponding diethyl acetal 9.This compound was the starting material in the synthesis of the suicide precursor 8, featuring a reductive amination leading to 12 and a Lewis-acid-catalysed cyclization giving 8.

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