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3783-61-7

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3783-61-7 Usage

General Description

N-(2-Ethoxy-2-oxoethyl)-beta-alanine ethyl ester is a chemical compound that belongs to the class of beta-alanine derivatives. It is an ethyl ester of beta-alanine, which is an amino acid that is known to help in the production of carnosine in the body. Carnosine is an important compound for muscle function and may have antioxidant properties as well. N-(2-ethoxy-2-oxoethyl)-beta-alanine ethyl ester is used in the pharmaceutical and research industries for its potential role in improving muscle performance and endurance, as well as its possible antioxidant effects.

Check Digit Verification of cas no

The CAS Registry Mumber 3783-61-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,8 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3783-61:
(6*3)+(5*7)+(4*8)+(3*3)+(2*6)+(1*1)=107
107 % 10 = 7
So 3783-61-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO4/c1-3-13-8(11)5-6-10-7-9(12)14-4-2/h10H,3-7H2,1-2H3

3783-61-7SDS

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 ethyl 3-[(2-ethoxy-2-oxoethyl)amino]propanoate

1.2 Other means of identification

Product number -
Other names Ethyl 3-(ethoxycarbonylmethylamino)propionate

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:3783-61-7 SDS

3783-61-7Relevant articles and documents

AN IMPROVED PROCESS FOR THE PREPARATION OF UPADACITINIB INTERMEDIATE

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Page/Page column 5-6, (2022/03/09)

The present invention provides an improved process for the preparation of upadacitinib of intermediate of formula II by reacting formula B with Grignard reagent in presence of an Iron catalyst.

Practical synthesis of ethyl 3-fluoro-1-pyrrole-2-carboxylate: A key fragment of a potent drug candidate against hepatitis b virus

René, Adeline,Quilan, Maxime,Deng, Yicheng,Cheng, Yang,Teleha, Christopher A.,Raboisson, Pierre,Bonfanti, Jean-Fran?ois,Fortin, Jér?me,Charette, André. B.,Pannecoucke, Xavier,Poisson, Thomas,Jubault, Philippe

, p. 792 - 801 (2019/10/16)

We report herein the development of two efficient synthetic routes for the preparation of a key fragment required for the synthesis of potent drug candidates of Hepatitis B virus. The ethyl 3-fluoro-1-H-pyrrole-2-carboxylate scaffold was synthesized from readily available starting materials in good overall yields. The scalability of one of the developed routes was demonstrated and afforded the desired target in good yield and excellent purity (99%).

GNAQ targeted dsRNA compositions and methods for inhibiting expression

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Page/Page column 41, (2017/03/08)

The invention relates to a double-stranded ribonucleic acid (dsRNA) targeting a G-alpha q subunit (GNAQ) of a heterotrimeric G gene, and methods of using the dsRNA to inhibit expression of GNAQ.

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