179003-02-2

Basic information

• Product Name: methyl 3-(2-(tert-butoxycarbonyl)aminoethyl)benzoate
• Synonyms: methyl 3-(2-(tert-butoxycarbonyl)aminoethyl)benzoate
• CAS NO: 179003-02-2
• Molecular Weight: 279.336
• Mol File: 179003-02-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: methyl 3-(2-(tert-butoxycarbonyl)aminoethyl)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-(2-(tert-butoxycarbonyl)aminoethyl)benzoate(179003-02-2)
• EPA Substance Registry System: methyl 3-(2-(tert-butoxycarbonyl)aminoethyl)benzoate(179003-02-2)

Safety Data

• Hazardous Substances Data: 179003-02-2(Hazardous Substances Data)

Upstream product

• 7150-72-3 t-butyl N-vinylcarbamate 
• 618-91-7 methyl 3-iodo-benzoate 
• 68432-92-8 methyl 3-cyanomethylbenzoate 
• 1129-28-8 3-methoxycarbonylbenzyl bromide 
• 24424-99-5 di-tert-butyl dicarbonate 
• 179003-00-0 3-(2-Amino-ethyl)-benzoic acid methyl ester 

Downstream Products

• 1093938-76-1 methyl 3-(2-(tert-butoxycarbonyl(methyl)amino)ethyl)benzoate 

Relevant articles and documents

Hybrid Organic Lead Iodides: Role of Organic Cation Structure in Obtaining 1D Chains of Face-Sharing Octahedra vs 2D Perovskites

((R(CH2)nNH3+ cations (R = aryl, substituted cyclohexyl; n = 1, 2) can form hybrid lead iodides that include both 2D layered perovskites of formula [R(CH2)nNH3]2PbI4 and 1D structures consisting of 1D wires of face-sharing PbI6 octahedra and having the formula [R(CH2)nNH3]PbI3 (face-sharing lead iodide chains, FSLICs). Using a series of such cations, we find that 1D FSLIC formation is favored when hydrogen bonding is possible between the ammonium moiety of one cation and a hydrogen-bond acceptor substituent of the same or another cation. A total of 16 new hybrid organic lead iodide crystal structures, 11 of which are FSLICs, are reported. The FSLIC structures can be further categorized according to the arrangement of neighboring wires. The optical properties of these materials are largely insensitive to the identity of the organic cations and to the resulting structural details. However, there is a correlation between the exciton energy and the pattern in which the wires are arranged relative to one another. Density functional theory calculations indicate that the dispersion at the top of the valence band varies depending on the relative wire arrangement.

HIGHLY WATER-SOLUBLE SALTS OF A SHORT ACTING PHENYLALKYLAMINE CALCIUM CHANNEL BLOCKER AND USES THEREOF

The present invention includes surprisingly water-soluble salts of a phenylalkylamine compound that are potent antagonists of L-type calcium channels. Aqueous solutions including salts of the instant invention are formulated for nasal administration and provide a novel therapeutic platform for the treatment of stable angina, migraine, and cardiac arrhythmia, such as paroxysmal supraventricular tachycardia.

Aromatic compounds containing basic and acidic termini useful as fibrinogen receptor antagonists

This invention relates to novel compounds containing basic and acidic termini, pharmaceutical compositions containing such compounds, processes for preparing such compounds, and to methods of using these compounds, alone or in combination with other therapeutic agents, for the inhibition of platelet aggregation, as thrombolytics, and/or for the treatment of thromboembolic disorders.