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Ethanimidic acid, 2-[[(phenylmethoxy)carbonyl]amino]-, ethyl ester, also known as ethyl 2-[(phenylmethoxy)carbonyl]amino]acetate, is a chemical compound with the molecular formula C11H14N2O4. It is a derivative of ethanimidic acid, featuring an ethyl ester group and a phenylmethoxycarbonyl moiety. Ethanimidic acid, 2-[[(phenylmethoxy)carbonyl]amino]-, ethyl ester is characterized by its amide and ester functional groups, which contribute to its reactivity and potential applications in organic synthesis. It is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its ability to form stable intermediates in peptide bond formation and other chemical reactions. The compound's structure allows for further functionalization and modification, making it a versatile building block in the development of new molecules with specific properties and applications.

1755-98-2

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1755-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1755-98-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1755-98:
(6*1)+(5*7)+(4*5)+(3*5)+(2*9)+(1*8)=102
102 % 10 = 2
So 1755-98-2 is a valid CAS Registry Number.

1755-98-2SDS

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 2-{[(benzyloxy)carbonyl]amino}ethanimidate

1.2 Other means of identification

Product number -
Other names ethyl 2-phenylmethoxycarbonylaminoethanimidate

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:1755-98-2 SDS

1755-98-2Relevant academic research and scientific papers

UREA DERIVATIVES AS PYRUVATE KINASE ACTIVATORS

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, (2022/02/15)

The subject matter described herein is directed to pyruvate kinase activating compounds of Formula I and pharmaceutical salts thereof, methods of preparing the compounds, pharmaceutical compositions comprising the compounds and methods of administering the compounds for the treatment of diseases associated with PKR and/or PKM2, such as pyruvate kinase deficiency, sickle cell disease, and beta-thalassemia.

HETEROCYCLIC COMPOUNDS AND USE THEREOF

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Page/Page column 34, (2018/08/03)

Heterocyclic compounds of Formula (I) shown herein. Also disclosed is a pharmaceutical composition containing one of the heterocyclic compounds. Further disclosed are methods of using one of the heterocyclic compounds for mobilizing hematopoietic stem cells and endothelial progenitor cells into the peripheral circulation, and for treating tissue injury, cancer, inflammatory disease, and autoimmune disease.

Inverse Electron Demand Diels-Alder Reactions of Indole IV. A New Route to β-Carbolines

Fan, Wen-Hong,Parikh, Mamta,Snyder, John K.

, p. 6591 - 6594 (2007/10/02)

β-Carbolines have been prepared by the intramolecular cycloaddition of indole with 1,2,4-triazines tethered from C3 with the indolyl nitrogen using a thiourea linkage.Subsequent to the cycloaddition, reductive cleavage of the thiourea subunit provides the β-carboline.

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