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[S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid is a unique chemical compound that features an amino acid with a distinctive structure. It is composed of an amino group, a butenoic acid group, and an ethoxy group, which collectively contribute to its versatility and potential applications across various domains. This molecule has garnered significant interest in the realms of biochemistry and pharmaceutical research, primarily due to its capacity to act as a foundational component in the creation of innovative drugs and therapeutic agents. The specific characteristics and potential biological activities of [S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid render it a subject worthy of further investigation and study.

49669-74-1

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49669-74-1 Usage

Uses

Used in Pharmaceutical Research and Development:
[S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid is utilized as a building block in the pharmaceutical industry for the development of new drugs and therapeutic agents. Its unique structure and properties make it a promising candidate for the creation of novel compounds with potential medicinal applications.
Used in Biochemical Studies:
In the field of biochemistry, [S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid is employed as a subject of study to explore its potential biological activities and interactions with other molecules. This research can lead to a better understanding of its role in biological systems and the discovery of new applications in medicine and other related fields.
Used in Drug Design and Synthesis:
[S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid is used as a key component in drug design and synthesis processes. Its incorporation into new molecular structures can enhance the efficacy and selectivity of drugs, potentially leading to the development of more effective treatments for various diseases and conditions.
Used in Chemical Synthesis for Diverse Applications:
Beyond the pharmaceutical and biochemical fields, [S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid can be utilized in chemical synthesis for a variety of applications. Its unique structure allows for the creation of new compounds that can be applied in industries such as materials science, agriculture, and environmental science, among others.

Check Digit Verification of cas no

The CAS Registry Mumber 49669-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,6 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 49669-74:
(7*4)+(6*9)+(5*6)+(4*6)+(3*9)+(2*7)+(1*4)=181
181 % 10 = 1
So 49669-74-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N2O3/c7-2-4-11-3-1-5(8)6(9)10/h1,3,5H,2,4,7-8H2,(H,9,10)/b3-1+/t5-/m0/s1

49669-74-1SDS

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 aviglycine

1.2 Other means of identification

Product number -
Other names Ro-4468

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:49669-74-1 SDS

49669-74-1Upstream product

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