116435-51-9

Basic information

• Product Name: (S)-3-bromo-heptane
• CAS NO: 116435-51-9
• Molecular Weight: 179.1
• Mol File: 116435-51-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (S)-3-bromo-heptane(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-bromo-heptane(116435-51-9)
• EPA Substance Registry System: (S)-3-bromo-heptane(116435-51-9)

Safety Data

• Hazardous Substances Data: 116435-51-9(Hazardous Substances Data)

Upstream product

• 589-82-2 heptan-3-ol 
• 142-82-5 n-heptane 
• 26549-25-7 S-(+)-3-heptanol 
• 56-23-5 tetrachloromethane 
• 72377-05-0 (2S)-ethylhexanoic acid 
• 7726-95-6 bromine 
• 10035-10-6 hydrogen bromide 

Downstream Products

• 7069-15-0 4-(1-ethyl-pentyl)-anisole 
• 3525-25-5 (3S)-3-Ethylheptan-1-ol 
• 116454-37-6 2-methylheptanoic acid 
• 124-07-2 Octanoic acid 
• 3780-58-3 3-methylhexanoic acid 
• 1185-39-3 2,2-dimethyl-n-valeric acid 
• 946760-77-6 4-(1-ethyl-pentyloxy)-phenylamine 
• 1580471-25-5 (E)-(3-ethylhept-1-en-1-yl)benzene 
• 42036-73-7 1-((E)-non-1-enyl)benzene 
• 14272-47-0 3-ethylheptanoic acid 
• 41887-57-4 3-Formylrifamycin SV O-n-Hept-3-yloxim 

Relevant articles and documents

Highly efficient oxidative bromination of alkanes with the HBr-H 2O2 system in the presence of catalyst

Various cycloalkanes and straight-chain alkanes were efficiently brominated with an aqueous HBr-H2O2 system. This oxidative brominating process was promoted by catalysis and irradiation with light. The cycloalkanes were converted to the corresponding bromo-cycloalkanes in moderate yields and the straight-chain alkanes produced dominantly secondary bromides. This simple but effective bromination method of alkanes is characterized by high atom efficiency, inexpensive reagents and the absence of organic waste, which make it a good alternative to the existing method for Ci￡H activation through bromination. A simple, effective, environmentally friendly method was researched for bromination of alkanes in good yield with HBr as the origin of bromine.

Direct bromination and iodination of non-activated alkanes by hypohalite reagents

The direct functionalisation of alkanes through bromination and iodination has been successfully achieved. The combination of stoichiometric mixtures of elemental halogen and sodium alkoxides leads to the formation of alkyl hypobromites and hypoiodites as reagents. The halogenation occurs without external photostimulation under thermal reaction conditions. Georg Thieme Verlag Stuttgart.

ANOMALOUS ORIENTATION EFFECTS DURING BENZOYLOXYLATIONS BY "SILVER BROMIDE DIBENZOATE"

The solid complex formed from bromine and silver benzoate reacts with both arenes and alkenes to form aryl and alkyl benzoates, respectively.Highly unusual substituent effects are observed in the benzoyloxylations of arenes.Electron-withdrawing groups (e.g. -NO2, -CN,-CO-) on the aromatic ring facilitate reaction though directing the attacking reagent exclusively to the meta position.In alkanes, tertiary positions are most prone to attack.