76-29-9

Basic information

• Product Name: D-3-BROMOCAMPHOR
• Synonyms: 2-Bornanone, 3-bromo-;3-bromo-1,7,7-trimethyl-bicyclo(2.2.1)heptan-2-on;3-bromo-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-on;3-bromo-2-bornanon;3-Bromo-2-bornanone;3-bromo-campho;Bicyclo[2.2.1]heptan-2-one, 3-bromo-1,7,7-trimethyl-;bicyclo[2.2.1]heptan-2-one,3-bromo-1,7,7-trimethyl-
• CAS NO: 76-29-9
• Molecular Formula: C10H15BrO
• Molecular Weight: 231.13
• EINECS: 200-950-8
• Mol File: 76-29-9.mol
• Article Data: 7

Chemical Properties

• Melting Point: 75-77°C
• Boiling Point: 274°C (rough estimate)
• Flash Point: 35.8 °C
• Appearance: /
• Density: 1,449 g/cm3
• Vapor Pressure: 0.0284mmHg at 25°C
• Refractive Index: 1.5290 (estimate)
• CAS DataBase Reference: D-3-BROMOCAMPHOR(CAS DataBase Reference)
• NIST Chemistry Reference: D-3-BROMOCAMPHOR(76-29-9)
• EPA Substance Registry System: D-3-BROMOCAMPHOR(76-29-9)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 76-29-9(Hazardous Substances Data)

Usage

General Description

D-3-Bromocamphor, also known as 3-Bromocamphor, is a chemical compound with the molecular formula C10H15BrO and the IUPAC name (1R,4R)-4-bromo-2,2-dimethyl-5,6,6-trimethylbicyclo[3.1.1]heptan-3-one. It is a chiral compound with a camphor-like structure and is commonly used as a reagent in organic synthesis. 3-Bromocamphor is also known for its insecticidal properties and has been used as an ingredient in some insect repellents and pesticides. It is considered to be a moderately toxic compound, and proper safety precautions should be taken when handling it.

InChI:InChI=1/C10H15BrO/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6-7H,4-5H2,1-3H3

Upstream product

• 60-29-7 diethyl ether 
• 514-12-5 3,3-dibromo-bornan-2-one 
• 464-48-2 (1S)-camphor 
• 56613-17-3 1,7,7-trimethyl-2-trimethylsilyloxy<2.2.1>bicyclohept-2-ene 
• 76-29-9 3-bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 76-22-2 Camphor 
• 736109-58-3 1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one 
• 78339-66-9 3-bromoborneol 
• 64-17-5 ethanol 
• 464-49-3 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 103502-25-6 2-bromo-4,7,7-trimethyl-3-oxo-norbornane-2-carbaldehyde 
• 87479-91-2 3-formyl-(+)-camphor 
• 7732-18-5 water 
• 7726-95-6 bromine 

Downstream Products

• 25611-66-9 4,7,7,4',7',7'-hexamethyl-[2,2']binorbornyl-3,3'-dione 
• 514-12-5 3,3-dibromocamphor 
• 854877-87-5 3-bromo-3-nitro-bornan-2-one 
• 514-12-5 3,3-dibromo-bornan-2-one 
• 95442-26-5 3-(α-hydroxy-benzhydryl)-1,7,7-trimethyl-norbornan-2-one 
• 1212173-15-3 3-acetyl-dl-camphor 
• 6624-51-7 camphorquinone dioxime 
• 67999-30-8 (1S,3S,4S)-3-bromocamphor-10-sulfonic acid 
• 5344-58-1 (1R)-3endo-bromo-2-oxo-bornane-8-sulfonic acid 
• 736109-58-3 1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one 
• 76-22-2 Camphor 
• 10293-10-4 rac-3,9-dibromocamphor 
• 464-48-2 (1S)-camphor 
• 759457-76-6 N-isobornylaniline 

Relevant articles and documents

Proton Resonance Spectra and Substituent-Induced Chemical Shifts of 3-Halocamphors

Complete signal assignments of high-field 1H NMR spectra for 3-halosubstituted camphors (endo and exo) are presented, allowing a refinement of a previous analysis for the chloro (endo and exo) and bromo (endo) derivatives.In addition, still unpublished data for the dichloro and exo-fluoro derivatives and for three new compounds (endo-fluoro, endo- and exo-iodo), in addition to a revised assignment of the camphor parent molecule, are reported.The precise substituent-induced chemical shifts (SCS) obtained for these difunctional systems are examined on the basis of well known transmission mechanisms aided by correlations with steric and electronic parameters, and taking into account SCS data from monohaloalkanes and the calculated molecular geometry data (using the AM1 method). - Keywords: 1H NMR 3-Halocamphors COSY-45 Molecular geometries Substituent-induced chemical shifts

A phenanthroline-derived ligand and its complexation with Pd(II): From ligand design, synthesis and Pd(II) complexes structures to its application

A novel phenanthroline-derived bis-opened-triazine ligand for selective complexation with Pd(ii) over 19 typical metals from HNO3 media was designed based on cavity modulation strategy. Structures of the three species of the Pd(ii) complexes of with the ligand were elucidated by 1H NMR titration isothermal titration calorimetry (ITC) and density functional theory (DFT) studies. ITC test and binding energy calculations demonstrated that the asymmetrical 1:1 Pd(ii)-ligand complex with a monodentate nitrate anion was the most stable among these three species of the Pd(ii) complexes. The excellent kinetics of Pd(ii) extraction with the ligand is due to its optimal conformation completely ready for metal ligation. The enhanced special extraction selectivity and fast extraction rate towards Pd(ii) achieved by the phenanthroline-derived ligand demonstrated that the effective separation of some radionuclides with smaller radius in HLW through cavity modulation strategy is a feasible approach.

Catalyst-free selective oxidation of alcohols to carbonyls using trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane as an efficient oxidant

A simple and efficient method for the selective oxidation of alcohols to ketones using trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane at room temperature is developed. The reactions were smoothly proceeded under catalyst-free conditions to provide ketones in quantitative yields within short reaction times. Also, this method is compatible with many functional groups including aldehydes, olefins, halogens, amines and esters. Graphical Abstract: [Figure not available: see fulltext.]