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3-amino-3-(2H-tetrazol-5-yl)propanoic acid is a chemical compound with the molecular formula C4H7N3O2. It is a derivative of amino acids, featuring a 2H-tetrazol-5-yl group attached to the propanoic acid backbone. 3-amino-3-(2H-tetrazol-5-yl)propanoic acid is known for its unique chemical properties, which include the presence of a tetrazol-5-yl ring, a five-membered aromatic ring with four nitrogen atoms and one hydrogen atom. The amino group and the carboxylic acid group are key functional groups in this molecule, which contribute to its reactivity and potential applications in various chemical and biological processes. The compound may be used in the synthesis of pharmaceuticals, agrochemicals, or as a building block in the creation of more complex molecules. Its specific applications and properties would depend on the context in which it is used, and further research would be needed to explore its full potential.

51163-38-3

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51163-38-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51163-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,6 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 51163-38:
(7*5)+(6*1)+(5*1)+(4*6)+(3*3)+(2*3)+(1*8)=93
93 % 10 = 3
So 51163-38-3 is a valid CAS Registry Number.

51163-38-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-3-(2H-tetrazol-5-yl)propanoic acid

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

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More Details:51163-38-3 SDS

51163-38-3Upstream product

51163-38-3Downstream Products

51163-38-3Relevant academic research and scientific papers

α-Amino Acid-Isosteric α-Amino Tetrazoles

Zhao, Ting,Kurpiewska, Katarzyna,Kalinowska-T?us?cik, Justyna,Herdtweck, Eberhardt,D?mling, Alexander

supporting information, p. 3009 - 3018 (2016/03/26)

The synthesis of all 20 common natural proteinogenic and 4 otherα-amino acid-isosteric α-amino tetrazoles has been accomplished, whereby the carboxyl group is replaced by the isosteric 5-tetrazolyl group. The short process involves the use of the key Ugi tetrazole reaction followed by deprotection chemistries. The tetrazole group is bioisosteric to the carboxylic acid and is widely used in medicinal chemistry and drug design. Surprisingly, several of the common α-amino acid-isosteric α-amino tetrazoles are unknown up to now. Therefore a rapid synthetic access to this compound class and non-natural derivatives is of high interest to advance the field.

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