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1H-1,2,4-Triazole-3-acetic acid, 5-amino-, ethyl ester is a chemical compound with the molecular formula C6H8N4O2. It is a versatile building block in the pharmaceutical industry, known for its potential biological activities such as anti-inflammatory, anti-cancer, and anti-fungal properties.
Used in Pharmaceutical Industry:
1H-1,2,4-Triazole-3-acetic acid, 5-amino-, ethyl ester is used as a building block for the synthesis of various pharmaceutical compounds due to its versatile nature and potential therapeutic benefits.
Used in Drug Development and Research:
1H-1,2,4-Triazole-3-acetic acid, 5-amino-, ethyl ester is used as a valuable component in drug development and research for its potential biological activities, including anti-inflammatory, anti-cancer, and anti-fungal properties.

86152-46-7

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86152-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86152-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,5 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86152-46:
(7*8)+(6*6)+(5*1)+(4*5)+(3*2)+(2*4)+(1*6)=137
137 % 10 = 7
So 86152-46-7 is a valid CAS Registry Number.

86152-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(3-amino-1H-1,2,4-triazol-5-yl)acetate

1.2 Other means of identification

Product number -
Other names ethyl (5-amino-1H-1,2,4-triazol-3-yl)acetate

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:86152-46-7 SDS

86152-46-7Relevant academic research and scientific papers

SYNTHESIS OF C-AZOYLACETIC ACID ESTERS BASED ON CARBETHOXYETHYLACETIMIDATE

Kiseleva, V. V.,Gakh, A. A.,Fainzil'berg, A. A.

, p. 1888 - 1895 (1990)

Preparative methods were developed for synthesizing 1,2,4-triazolyl-1,3,4-oxadiazolyl-, 1,2,4-oxadiazolyl-, and 1,3,4-thiadiazolylacetic acid esters based on carbethoxyethylacetimidate chlorohydrate.

Trinitromethyl-substituted 5-nitro- or 3-azo-1,2,4-triazoles: Synthesis, characterization, and energetic properties

Thottempudi, Venugopal,Gao, Haixiang,Shreeve, Jeanne M.

experimental part, p. 6464 - 6471 (2011/06/10)

Various new polynitro-1,2,4-triazoles containing a trinitromethyl group were synthesized by straightforward routes. These high nitrogen and oxygen-rich compounds were fully characterized using IR and multinuclear NMR spectroscopy, elemental analysis, natural bonding orbital (NBO) analysis, and differential scanning calorimetry (DSC) and, in the case of 12, with single crystal X-ray structuring. The heats of formation for all compounds were calculated with Gaussian 03 (revision D.01) and then combined with experimentally determined densities to determine detonation pressures (P) and velocities (D) of the energetic materials (Cheetah 5.0). They exhibit high density, good thermal stability, acceptable oxygen balance, positive heat of formation, and excellent detonation properties, which, in some cases, are superior to those of TNT, RDX, and HMX.

Design, synthesis and molecular modeling study of acylated 1,2,4-triazole-3-acetates with potential anti-inflammatory activity

Abdel-Megeed, Ashraf M.,Abdel-Rahman, Hamdy M.,Alkaramany, Gamal-Eldien S.,El-Gendy, Mahmoud A.

experimental part, p. 117 - 123 (2009/04/07)

The present investigation is concerned with the synthesis of different acylated 1,2,4-triazole-3-acetates with the objective of discovering novel and potent anti-inflammatory agents. Structures of the synthesized compounds were elucidated by spectral and

Synthesis of esters and amides of 5-amino-1,2,4-triazole-3-carboxylic and 5-amino-1,2,4-triazol-3-ylacetic acids

Chernyshev,Chernysheva,Taranushich

, p. 783 - 786 (2008/02/05)

Various synthetic routes to esters and amides of 5-amino-1,2,4-triazole-3- carboxylic and 5-amino-1,2,4-triazol-3-ylacetic acids were examined. Pleiades Publishing, Inc., 2006.

Synthesis and Some Transformations of 3-Substituted 1,2,4-Triazole-5-acetic Acids

Kofman, T. P.,Uvarova, T. A.,Kartseva, G. Yu.

, p. 240 - 244 (2007/10/02)

The reaction of aminoguanidine hydrogen carbonate with malonic acid gave 5-amino-1,2,4-triazole-5-acetic acid whose further transformations resulted in azo and nitro 1,2,4-triazole derivatives containing carboxy and ethoxycarbonylmethyl groups at the ring carbon atom; their nitrosation afforded derivatives of 3-nitro-1,2,4-triazol-5-yl(hydroxyimino)acetic acid.

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