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4-[2-amino-2-(2H-tetrazol-5-yl)ethyl]phenol is a complex organic compound with the molecular formula C10H12N4O. It features a phenol group (a hydroxyl group attached to a benzene ring), an amino group, and a 2H-tetrazol-5-ylethyl group. The tetrazol-5-ylethyl moiety consists of a tetrazol ring (a five-membered ring with four nitrogen atoms) attached to an ethyl chain. This chemical is known for its potential applications in pharmaceuticals and as a building block in the synthesis of various compounds due to its unique structure and reactivity. It is important to note that handling and use of such chemicals should be done with caution, following appropriate safety protocols, as they may have specific toxicological profiles or reactivity concerns.

56876-28-9

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56876-28-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56876-28-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,7 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56876-28:
(7*5)+(6*6)+(5*8)+(4*7)+(3*6)+(2*2)+(1*8)=169
169 % 10 = 9
So 56876-28-9 is a valid CAS Registry Number.

56876-28-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-amino-2-(2H-tetrazol-5-yl)ethyl]phenol

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:56876-28-9 SDS

56876-28-9Downstream Products

56876-28-9Relevant academic research and scientific papers

Antileukemic activity of tetrazole analogs of phenylalanine derivatives

Darling

, p. 356 - 358 (1982)

Eleven tetrazole analogs of substituted phenylalanines were prepared and tested for antitumor activity using P-388 lymphocytic leukemia cells in mice. None of the compounds exhibited significant activity (T/C%, 125).

α-Amino Acid-Isosteric α-Amino Tetrazoles

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

, 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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