1-Bromoadamantane CAS 768-90-1 Purity >99.0% (GC)
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Chemical Name | 1-Bromoadamantane |
Synonyms | 1-Adamantyl Bromide |
CAS Number | 768-90-1 |
CAT Number | RF-PI2306 |
Stock Status | In Stock, Production Capacity 35 MT/Month |
Molecular Formula | C10H15Br |
Molecular Weight | 215.13 |
Melting Point | 118.0 to 121.0℃ |
Sensitive | Moisture & Light & Air Sensitive |
Solubility in Water | Soluble in Organic Solvents and Insoluble in Water |
Stability | Stable Under Normal Temperatures and Pressures |
Brand | Ruifu Chemical |
Item | Specifications |
Appearance | White to Light Yellow to Light Brown Powder |
Purity / Analysis Method | >99.0% (GC) |
Loss on Drying | <1.00% |
Residue on Ignition | <0.50% |
Total Impurities | <1.00% |
Solubility in Methanol | Almost Transparency |
Heavy Metals (as Pb) | <0.002% |
Infrared Spectrum | Conforms to Structure |
Proton NMR Spectrum | Conforms to Structure |
Test Standard | Enterprise Standard |
Usage | Pharmaceutical Intermediates |
Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement
Storage Condition: Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. Store protected from moisture
1-Bromoadamantane (CAS: 768-90-1) is an important intermediate, used in synthesizing medicines and new materials etc. Used as pharmaceutical intermediates, is the synthesis of amantane salt intermediates. 1-Bromoadamantane is an important intermediate for the synthesis of Amantadine Hydrochloride, Amantadine Hydrochloride as an anti-drug and drug effects, for the prevention and treatment of A2 influenza in Asia. It is an synthetic intermediate of 1-Adamantanamine Hydrochloride. 1-Bromoadamantane shows some anti-viral activity due to the adamantane structure. In addition it shows anti-microbial activity and cytotoxic application. 1-Bromoadamantane was used in the synthesis of a new organic–organic nanoscale composite thin-film dielectric. 1-Bromoadamantane forms inclusion complexes with α-, β-, and γ-cyclodextrins. It causes the alkylation of Co(II) complexes of β-diketones.