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1H-Imidazole-2-carboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-1-methyl-, ethyl ester is a chemical compound with the molecular formula C13H21N3O4. It is an ester derivative of 1H-imidazole-2-carboxylic acid, a heterocyclic compound featuring an imidazole ring. This ethyl ester form is widely utilized in organic synthesis and pharmaceutical research, serving as a reagent or intermediate in the production of various drugs and biologically active compounds. The imidazole ring endows 1H-IMidazole-2-carboxylic acid, 4-[[(1,1-diMethylethoxy)carbonyl]aMino]-1-Methyl-, ethyl ester with unique chemical and biological properties, rendering it valuable for diverse applications in medicinal chemistry and drug development.

128293-63-0

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128293-63-0 Usage

Uses

Used in Pharmaceutical Research:
1H-Imidazole-2-carboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-1-methyl-, ethyl ester is used as a reagent in pharmaceutical research for its unique chemical and biological properties. It aids in the synthesis of various drugs and biologically active compounds, contributing to the development of novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 1H-Imidazole-2-carboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-1-methyl-, ethyl ester is employed as an intermediate. Its presence in the synthesis process allows for the creation of complex organic molecules, facilitating advancements in chemical research and the production of new materials.
Used in Medicinal Chemistry:
1H-Imidazole-2-carboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-1-methyl-, ethyl ester is utilized in medicinal chemistry for its potential to contribute to the discovery and design of new pharmaceuticals. Its unique structure and properties make it a promising candidate for the development of drugs targeting specific biological pathways or receptors.
Used in Drug Development:
In the industry of drug development, 1H-Imidazole-2-carboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-1-methyl-, ethyl ester is used as a key component in the formulation of new drugs. Its versatility and reactivity in chemical reactions enable the creation of innovative pharmaceuticals with improved efficacy and safety profiles.
Used in Chemical Research:
1H-Imidazole-2-carboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-1-methyl-, ethyl ester is also used in chemical research to explore its properties and potential applications. Understanding its reactivity, stability, and interactions with other molecules can lead to new insights and discoveries in the realm of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 128293-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,2,9 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 128293-63:
(8*1)+(7*2)+(6*8)+(5*2)+(4*9)+(3*3)+(2*6)+(1*3)=140
140 % 10 = 0
So 128293-63-0 is a valid CAS Registry Number.

128293-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-methyl-4-[(2-methylpropan-2-yl)oxycarbonylamino]imidazole-2-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 4-tert-butyloxycarbonylamino-1-methylimidazole-2-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:128293-63-0 SDS

128293-63-0Relevant academic research and scientific papers

Solid phase synthesis of polyamides containing imidazole and pyrrole amino acids

Baird, Eldon E.,Dervan, Peter B.

, p. 6141 - 6146 (2007/10/03)

The solid phase synthesis of sequence specific DNA binding polyamides containing N-methylimidazole (Im) and N-methylpyrrole (Py) amino acids is described. Two monomer building blocks, Boc-Py-OBt ester and Boc-Im acid, are prepared on a 50 g scale without column chromatography. Using commercially available Boc-β-alanine-Pam resin, cycling protocols were optimized to afford high stepwise coupling yields (>99%). Deprotection by aminolysis affords up to 100 mg quantities of polyamide. Solid phase methodology increases both the number and complexity of minor groove binding polyamides which can be synthesized and analyzed with regard to DNA binding affinity and sequence specificity. The solid phase synthesis of a representative eight-residue polyamide is reported.

The Preparation and Properties of Partially Protected 4-Amino-1-methylimidazole-2-carboxylic Acids to be Used as Intermediates in the Synthesis of Analogues of Distamycin A

Grehn, Leif,Ding, Lu,Ragnarsson, Ulf

, p. 67 - 74 (2007/10/02)

Partially protected 4-amino-1-methylimidazole-2-carboxylic acid derivatives have been prepared by a convenient route from the corresponding nitro analogue.Such derivatives, blocked on the amino function with tert-butyloxycarbonyl (4) or formyl groups (8)

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