1032350-06-3

Basic information

• Product Name: Tert-Butyl1-(4-Bromophenyl)cyclobutylcarbamate
• Synonyms: Tert-Butyl1-(4-Bromophenyl)cyclobutylcarbamate;tert-butyl N-[1-(4-bromophenyl)cyclobutyl]carbamate;1-(BOC-AMINO)-1-(4-BROMOPHENYL)-CYCLOBUTANE;[1-(4-bromophenyl)cyclobutyl]carbamic acid tert-butyl ester;2-Methyl-2-propanyl [1-(4-bromophenyl)cyclobutyl]carbamate
• CAS NO: 1032350-06-3
• Molecular Formula: C₁₅H₂₀BrNO₂
• Molecular Weight: 326.2288
• Mol File: 1032350-06-3.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 400.5±34.0 °C(Predicted)
• Appearance: /
• Density: 1.33±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 11.82±0.20(Predicted)
• CAS DataBase Reference: Tert-Butyl1-(4-Bromophenyl)cyclobutylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: Tert-Butyl1-(4-Bromophenyl)cyclobutylcarbamate(1032350-06-3)
• EPA Substance Registry System: Tert-Butyl1-(4-Bromophenyl)cyclobutylcarbamate(1032350-06-3)

Safety Data

• Hazardous Substances Data: 1032350-06-3(Hazardous Substances Data)

Usage

General Description

Tert-Butyl 1-(4-Bromophenyl)cyclobutylcarbamate is a type of chemical compound which falls under the category of carbamates. It is an organic compound composed of tertiary butyl, a bromophenyl group, and a cyclobutyl group, linked together with a carbamate functional group. Its primary structure includes a four-carbon, cyclobutyl ring appended with carbamate and bromophenyl substituents. Its properties, uses and protective measures can be determined by scientific study and research, but specific details on this particular compound may not be readily available due to its unique and complex structure. Like other carbamates, it may have potential applications in various fields such as pharmaceuticals and agrochemicals, depending on its reactivity and biological activity.

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 1094218-30-0 1-(4-bromophenyl)cyclobutanamine 
• 1193389-40-0 1-(4-bromophenyl)cyclobutane-1-amine hydrochloride 
• 16532-79-9 4-Bromophenylacetonitrile 
• 485828-58-8 1-(4- bromophenyl)cyclobutane-1-carbonitrile 
• 75-65-0 tert-butyl alcohol 
• 133017-10-4 Butyl 2-(4-bromophenyl)acetate 
• 1032350-05-2 1-(4-bromophenyl)cyclobutanecarboxylic acid amide 

Downstream Products

• 1032527-89-1 tert-butyl 1-(4-(phenylethynyl)phenyl)cyclobutylcarbamate 
• 1032528-06-5 {1-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert.-butyl ester 
• 1356002-02-2 tert-butyl {1-[4-(5-methyl-3-phenylimidazo[1,2-a]pyridin-2-yl)phenyl]cyclobutyl}carbamate 
• 1355999-68-6 1-[4-(5-methyl-3-phenylimidazo[1,2-a]pyridin-2-yl)phenyl]cyclobutanamine 
• 1247894-84-3 1-[4-(6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)phenyl]cyclobutylamine 
• 1355239-60-9 1-[4-(2-methyl-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)phenyl]cyclobutylamine 
• 1355239-62-1 {7-[4-(1-amino-cyclobutyl)phenyl]-6-phenyl-imidazo[1,2-a]pyrimidin-5-yl}cyclopropylamine 
• 1355239-74-5 {5-[4-(1-aminocyclobutyl)phenyl]-6-phenyl-2-pyridine-2-yl-[1,2,4]triazolo[1,5-a]pyrimidin-7-yl}tert-butylamine 
• 1355239-89-2 1-{4-[3-(4-methansulfonyl-phenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutylamine 
• 1247897-89-7 {1-[4-(3-bromo-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)phenyl]cyclobutyl}carbamic acid tert-butyl ester 
• 1355240-89-9 (1-{4-[3-(4-methanesulfonyl-phenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutyl)carbamic acid tert-butyl ester 
• 1355240-23-1 1-{4-[3-(4-fluorophenyl)-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl]phenyl}cyclobutylamine 
• 1355240-37-7 {1-[4-(2-methyl-6-phenyl-[1,2,4]triazolo[1,5-a]pyrimidin-5-yl)phenyl]cyclobutyl}carbamic acid tert-butyl ester 
• 1247897-86-4 {1-[4-(6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)phenyl]cyclobutyl}carbamic acid tert-butyl ester 

Relevant articles and documents

ISOQUINOLINE COMPOUNDS, A PROCESS FOR THEIR PREPARATION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

A compound of formula (I): wherein the substituents are as defined in the description. Medicinal products containing the same which are useful in treating or preventing pathologies which are the result of activation of the RhoA/ROCK pathway and phosphorylation of the myosin light chain.

PROCESS OF PREPARING 3-(3-(4-(1-AMINOCYCLOBUTYL)PHENYL)-5-PHENYL-3H-IMIDAZO[4,5-B]PYRIDIN-2-YL)PYRIDIN-2-AMINE

The present invention is directed to a processes for the synthesis of 3-(3-(4-(1-aminocyclobutyl)phenyl)-5-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-amine:

NOVEL IMIDAZO-OXAZINE COMPOUND OR SALT THEREOF

The present invention provides an imidazooxazine compound represented by Formula (I) or a salt thereof, wherein A, B, C, and D are as defined in the specification.