847416-99-3

Basic information

• Product Name: INDEX NAME NOT YET ASSIGNED
• Synonyms: 3-(Boc-aMino)cyclopentanone;ML213;(3-Oxo-cyclopentyl)-carbamic acid tert-butyl ester;1-(Boc-amino)-3-oxocyclopentane
• CAS NO: 847416-99-3
• Molecular Formula: C₁₀H₁₇NO₃
• Molecular Weight: 199.25
• Product Categories: CYCLOPENTANE
• Mol File: 847416-99-3.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 319.2±31.0 °C(Predicted)
• Appearance: /
• Density: 1.07±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 11.89±0.20(Predicted)
• CAS DataBase Reference: INDEX NAME NOT YET ASSIGNED(CAS DataBase Reference)
• NIST Chemistry Reference: INDEX NAME NOT YET ASSIGNED(847416-99-3)
• EPA Substance Registry System: INDEX NAME NOT YET ASSIGNED(847416-99-3)

Safety Data

• Hazardous Substances Data: 847416-99-3(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 1228748-71-7 3-amino cyclopentanone 
• 1154870-59-3 trans-(+/-)-(3-hydroxycyclopentyl)-carbamic acid,1,1-dimethylethyl ester 
• 13725-38-7 3-aminocyclopentan-1-ol 
• 930-30-3 cyclopent-2-enone 
• 4248-19-5 tert-butyl carbazate 
• 855863-93-3 3-tert-butoxycarbonylaminocyclopentanecarboxylic acid 

Downstream Products

• 154737-89-0 tert-butyl ((1S,3S)-3-hydroxycyclopentyl)carbamate 
• 1154870-59-3 (+/-)-tert-butyl (cis-3-hydroxycyclopentyl)carbamate 
• 1215071-23-0 tert-butyl (3,3-difluorocyclopentyl)carbamate 
• 1154870-59-3 trans-(+/-)-(3-hydroxycyclopentyl)-carbamic acid,1,1-dimethylethyl ester 
• 13725-38-7 3-aminocyclopentan-1-ol 
• 1408075-75-1 3-amino-1-methylcyclopentanol 
• 1197398-99-4 tert-butyl (3-aminocyclopentyl)carbamate 
• 1154870-59-3 (±)-trans-(3-hydroxycyclopentyl)carbamic acid tert-butyl ester 
• 1154870-59-3 (+/-)-cis-(3-hydroxy-cyclopentyl)-carbamic acid tert-butyl ester 
• 1643574-07-5 tert-butyl N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopent-3-en-1-yl]carbamate 
• 939398-48-8 3,3-difluorocyclopentan-1-amine hydrochloride 
• 946593-67-5 (1S,3S)-3-aminocyclopentan-1-ol 

Relevant articles and documents

Decarboxylative Oxygenation via Photoredox Catalysis

The direct conversion of aliphatic carboxylic acids to their dehomologated carbonyl analogues has been accomplished through photocatalytic decarboxylative oxygenation. This transformation is applicable to an array of carboxylic acid motifs, producing ketones, aldehydes, and amides in excellent yields. Preliminary results demonstrate that this methodology is further amenable to aldehyde substrates via in situ oxidation to the corresponding acid and subsequent decarboxylative oxygenation. We have exploited this strategy for the sequential oxidative dehomologation of linear aliphatic chains.

Novel indazoles for the treatment and prophylaxis of respiratory syncytial virus infection

The invention provides novel compounds having the general formula: wherein R1, R2, R3, R4, R5, R7, A1, A2 and A3 are as described herein, compositions including the compounds and methods of using the compounds.

TETRACYCLIC HETEROCYCLE COMPOUNDS USEFUL AS HIV INTEGRASE INHIBITORS

The present invention relates to Tetracyclic Heterocycle Compounds of Formula (I) and pharmaceutically acceptable salts or prodrug thereof, wherein n, X, Y, Z, R1, R2, and R3 are as defined herein. The present invention also relates to compositions comprising at least one Tetracyclic Heterocycle Compound, and methods of using the Tetracyclic Heterocycle Compounds for treating or preventing HIV infection in a subject.