877593-11-8

Basic information

• Product Name: (3-HYDROXYMETHYL-PYRIDIN-2-YL)-CARBAMIC ACID TERT-BUTYL ESTER
• Synonyms: TERT-BUTYL 3-(HYDROXYMETHYL)PYRIDIN-2-YLCARBAMATE;(3-HYDROXYMETHYL-PYRIDIN-2-YL)-CARBAMIC ACID TERT-BUTYL ESTER;tert-butyl N-[3-(hydroxyMethyl)pyridin-2-yl]carbaMate;2-(Boc-amino)-3-(hydroxymethyl)pyridine
• CAS NO: 877593-11-8
• Molecular Formula: C11H16N2O3
• Molecular Weight: 224.26
• Product Categories: pharmacetical
• Mol File: 877593-11-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: (3-HYDROXYMETHYL-PYRIDIN-2-YL)-CARBAMIC ACID TERT-BUTYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: (3-HYDROXYMETHYL-PYRIDIN-2-YL)-CARBAMIC ACID TERT-BUTYL ESTER(877593-11-8)
• EPA Substance Registry System: (3-HYDROXYMETHYL-PYRIDIN-2-YL)-CARBAMIC ACID TERT-BUTYL ESTER(877593-11-8)

Safety Data

• Hazardous Substances Data: 877593-11-8(Hazardous Substances Data)

Usage

Uses

(3-Hydroxymethylpyridin-2-yl)carbamic acid tert-butyl ester

Upstream product

• 877593-10-7 methyl 2-[bis(tert-butoxycarbonyl)amino]nicotinate 
• 5345-47-1 2-aminopyridin-3-carboxylic acid 
• 14667-47-1 methyl 2-aminonicotinate 
• 912369-42-7 methyl 3-{[(tert-butoxy)carbonyl]amino}pyridine-2-carboxylate 
• 873460-09-4 2-tert-butoxycarbonylamino-nicotinic acid methyl ester 

Downstream Products

• 10586-52-4 2-phenyl-1H-pyrrolo[2,3-b]pyridine 
• 139962-69-9 2-(4-Chloroyphenyl)<1H>-pyrrolo<2,3-b>pyridine 
• 139962-68-8 2-(4-Methoxyphenyl)<1H>-pyrrolo<2,3-b>pyridine 

Relevant articles and documents

Azaindole synthesis through dual activation catalysis with N-heterocyclic carbenes

A convergent, transition-metal-free synthesis of 2-aryl-azaindoles has been developed. The interception of a reactive aza-ortho-azaquinone methide intermediate by an acyl anion equivalent generated through carbene catalysis provides high yields, a wide substrate scope, and the synthesis of previously inaccessible azaindoles.

Preparation and chemical behavior of 2-(tert-butoxycarbonyl)amino-3- bromomethyl pyridine, a novel alkylating agent

Synthesis of a novel heterocyclic alkylating agent has been developed. Its instability toward elevated temperatures and/or polar media can be used to prepare 8-aza-1,4-dihydrobenzo[1,3-d]oxazin-2-one. Copyright Taylor & Francis LLC.