2534-90-9

Basic information

• Product Name: 2-bromobicyclo[2.2.1]heptane-1-carboxylic acid
• Synonyms: bicyclo[2.2.1]heptane-1-carboxylic acid, 2-bromo-
• CAS NO: 2534-90-9
• Molecular Formula: C₈H₁₁BrO₂
• Molecular Weight: 219.0757
• Mol File: 2534-90-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 314.1°C at 760 mmHg
• Flash Point: 143.8°C
• Density: 1.73g/cm³
• Vapor Pressure: 0.000103mmHg at 25°C
• Refractive Index: 1.614
• CAS DataBase Reference: 2-bromobicyclo[2.2.1]heptane-1-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromobicyclo[2.2.1]heptane-1-carboxylic acid(2534-90-9)
• EPA Substance Registry System: 2-bromobicyclo[2.2.1]heptane-1-carboxylic acid(2534-90-9)

Safety Data

• Hazardous Substances Data: 2534-90-9(Hazardous Substances Data)

Upstream product

• 934-28-1 norbornane-2-carboxylic acid 
• 1755-01-7 endo-Dicyclopentadien 
• 61242-71-5 (1R,2S,4S)-Bicyclo[2.2.1]heptane-2-carboxylic acid ethyl ester 
• 51789-95-8 bicyclo[2.2.1]hept-5-ene-endo-2-carboxylic acid ethyl ester 
• 19926-90-0 (+/-)-endo-bicyclo[2.2.1]hept-5-ene-2-carbaldehyde 
• 3574-54-7 2-endo-Bicyclo<2.2.1>heptanecarboxaldehyde 
• 18720-30-4 norbornane-1-carboxylic acid 
• 2534-71-6 (+/-)-2-bromo-norbornane-2endo-carboxylic acid 
• 934-29-2 acide bicyclo<2.2.1>heptane carboxylique-2 exo 
• 934-28-1 bicyclo(2.2.1)heptane-2-endo-carboxylic acid 
• 100379-07-5 2-exo-Bromobicyclo<2.2.1>heptane-2-endo-carboxaldehyde 

Downstream Products

• 41248-20-8 (+/-)-2-hydroxy-norbornane-2endo-carboxylic acid 
• 2534-77-2 exo-2-bromonorbornane 
• 104085-12-3 (1S,2S,4R)-2-Bromo-bicyclo[2.2.1]heptane-1-carboxylic acid ((R)-2-hydroxy-1-phenyl-ethyl)-amide 
• 104085-11-2 (1R,2R,4S)-2-Bromo-bicyclo[2.2.1]heptane-1-carboxylic acid ((R)-2-hydroxy-1-phenyl-ethyl)-amide 
• 149891-94-1 bicyclo<2.2.2>octane-1-carboxaldehyde-d tosylhydrazone 
• 7363-97-5 bicyclo<2.2.2>octane-1-carboxaldehyde tosylhydrazone 
• 2574-42-7 bicyclo<2.2.2>octane-1-methanol 
• 699-55-8 bicyclo[2.2.2]octane-1-carboxylic acid 
• 18720-30-4 norbornane-1-carboxylic acid 
• 2287-57-2 methyl bicyclo<2.2.1>heptane-1-carboxylate 
• 104085-16-7 (1S,2S,4R)-2-Bromo-bicyclo[2.2.1]heptane-1-carboxylic acid (R)-2-amino-2-phenyl-ethyl ester 
• 104085-15-6 (1R,2R,4S)-2-Bromo-bicyclo[2.2.1]heptane-1-carboxylic acid (R)-2-amino-2-phenyl-ethyl ester 
• 104085-13-4 (R)-2-((1R,2R,4S)-2-Bromo-bicyclo[2.2.1]hept-1-yl)-4-phenyl-4,5-dihydro-oxazole 
• 104085-14-5 (R)-2-((1S,2S,4R)-2-Bromo-bicyclo[2.2.1]hept-1-yl)-4-phenyl-4,5-dihydro-oxazole 

Relevant articles and documents

Protected amino hydroxy adamantane carboxylic acid and process for its preparation

Dipeptidyl peptidase IV (DP 4) inhibiting compounds are provided. The provided compounds can be used for treating diabetes and related diseases, especially Type II diabetes, and other diseases as set out herein, employing such DP 4 inhibitor or a combination of such DP 4 inhibitor and one or more of another antidiabetic agent such as metformin, glyburide, troglitazone, pioglitazone, rosiglitazone and/or insulin and/or one or more of a hypolipidemic agent and/or anti-obesity agent and/or other therapeutic agent.

Bicyclonon-1-ene: Matrix Isolation and Spectroscopic Characterization of a Moderately Strained Bridgehead Olefin

Bicyclonon-1-ene was generated in low-temperature matrices and in fluid solutions by photodecomposition of bicyclooct-1-yldiazomethane and its photorearrangement product, 3-(bicyclooct-1-yl)diazirine.It was characterized by IR and UV absorption and by 1H and 13C NMR spectroscopy.Further evidence for the proposed structure was provided by self-trapping and by the spectral effects of deuteration on the olefinic carbon.Observed IR spectra and isotopic shifts agree well with the results of semiempirical (MNDO) and ab initio (SCF/6-31G*) calculations.