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3-amino-3-(2H-tetrazol-5-yl)propanamide is a chemical compound with the molecular formula C4H8N4O. It is a derivative of propanamide, featuring an amino group (-NH2) and a 2H-tetrazol-5-yl group attached to the propane backbone. 3-amino-3-(2H-tetrazol-5-yl)propanamide is known for its potential applications in pharmaceuticals and chemical research, particularly in the development of drugs and other bioactive molecules. The presence of the tetrazol-5-yl group, which is a five-membered ring with four nitrogen atoms, contributes to its unique chemical properties and reactivity. The compound's structure allows for various functional group modifications, making it a versatile building block in organic synthesis and medicinal chemistry.

51163-39-4

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51163-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51163-39-4 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 51163-39:
(7*5)+(6*1)+(5*1)+(4*6)+(3*3)+(2*3)+(1*9)=94
94 % 10 = 4
So 51163-39-4 is a valid CAS Registry Number.

51163-39-4SDS

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)propanamide

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:51163-39-4 SDS

51163-39-4Upstream product

51163-39-4Downstream Products

51163-39-4Relevant 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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