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Ethyl 5-((tert-butoxycarbonylamino)methyl)-1,2,4-oxadiazole-3-carboxylate is a chemical compound characterized by its molecular formula C11H16N4O6. It is a derivative of the oxadiazole heterocyclic ring, which is a five-membered ring containing nitrogen and oxygen atoms. ethyl 5-((tert-butoxycarbonylamino)methyl)-1,2,4-oxadiazole-3-carboxylate is recognized for its potential biological activities and is often utilized as a building block in the synthesis of various drugs and agrochemicals. Its diverse pharmacological properties have made it a significant target for chemical and medicinal research.

164029-34-9

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164029-34-9 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 5-((tert-butoxycarbonylamino)methyl)-1,2,4-oxadiazole-3-carboxylate is used as a key intermediate in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs. Its unique structure allows for the creation of molecules with specific biological activities, making it valuable in drug discovery and medicinal chemistry.
Used in Agricultural Industry:
In the agricultural sector, ethyl 5-((tert-butoxycarbonylamino)methyl)-1,2,4-oxadiazole-3-carboxylate is employed as a building block in the synthesis of agrochemicals. Its incorporation into these compounds can enhance their effectiveness in pest control and crop protection, contributing to improved agricultural yields and sustainability.
Used in Chemical Research:
Ethyl 5-((tert-butoxycarbonylamino)methyl)-1,2,4-oxadiazole-3-carboxylate is utilized as a subject of study in chemical research to explore its diverse pharmacological properties. Researchers investigate its interactions with biological targets and its potential applications in the development of novel therapeutic agents and chemical entities with specific modes of action.

Check Digit Verification of cas no

The CAS Registry Mumber 164029-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,0,2 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 164029-34:
(8*1)+(7*6)+(6*4)+(5*0)+(4*2)+(3*9)+(2*3)+(1*4)=119
119 % 10 = 9
So 164029-34-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H17N3O5/c1-5-17-9(15)8-13-7(19-14-8)6-12-10(16)18-11(2,3)4/h5-6H2,1-4H3,(H,12,16)

164029-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-[[(2-methylpropan-2-yl)oxycarbonylamino]methyl]-1,2,4-oxadiazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl N-Boc-5-aminomethyl-1,2,4-oxadiazole-3-carboxylate

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:164029-34-9 SDS

164029-34-9Relevant academic research and scientific papers

Synthesis of 1,2,4-Oxadiazole-, 1,3,4-Oxadiazole-, and 1,2,4-Triazole-Derived Dipeptidomimetics

Borg, Susanna,Estenne-Bouhtou, Genevieve,Luthman, Kristina,Csoeregh, Ingeborg,Hesselink, Willy,Hacksell, Uli

, p. 3112 - 3120 (2007/10/02)

Three series of heterocyclic dipeptidomimetics have been synthesized.The compounds were designed as amino acid-glycine mimetics containing 1,2,4-oxadiazole, 1,3,4-oxadiazole, and 1,2,4-triazole ring systems, useful as building blocks in the synthesis of m

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