Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 768-95-6
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Aluminum Foil Bag, Drum
Delivery Time: 7-15 days
Payment Terms: T/T, L/C, D/A, Western Union
Supply Ability: TON
CAS NO:: |
768-95-6 |
Appearance :: |
White To Off-white Crystalline Powder |
Molecular Formula:: |
C10H16O |
Molecular Weight:: |
152.233 |
EINECS NO:: |
212-202-8 |
MDL NO:: |
MFCD00074729 |
CAS NO:: |
768-95-6 |
Appearance :: |
White To Off-white Crystalline Powder |
Molecular Formula:: |
C10H16O |
Molecular Weight:: |
152.233 |
EINECS NO:: |
212-202-8 |
MDL NO:: |
MFCD00074729 |
Product Description:
Product Name: 1-Adamantanol CAS NO: 768-95-6
Synonyms:
Tricyclo[3.3.1.13,7]decan-1-ol;
1-Adamantol;
1-adamantyl alcohol;
1-Hydroxyadamantane;
Chemical & Physical Properties:
Appearance : white to off-white crystalline powder.
Assay :≥99.0%
Density:1.16 g/cm3
Boiling Point:245.8℃ at 760 mmHg
Flash Point:240℃
Melting Point: 240℃
Water Solubility:Soluble in ethanol , methanol, and diethyl eth er. Partly miscible in water.
1-Adamantanol (English 1-Adamantanol) is also known as 1-hydroxy adamantane, 1-tricyclo[3.3.1.1(3.7)] decanol, soluble in organic solvents, insoluble in water, and sublimable. Used in the manufacture of synthetic adamantane derivatives and adabalin.
Reaction with vinylidene chloride can be 1-adamantane acetic acid. 1-adamantane acetic acid is then brominated and hydrolyzed to 3-hydroxy-1-adamantane acetic acid, and then reacted with vinylidene chloride to obtain 1,3-adamantane diacetic acid. 1-adamantanol and acetanilide undergo Friedel-Crafts alkylation reaction at room temperature in 98% sulfuric acid medium, and 1,3-bis(4-acetamidophenyl)adamantane can be directly synthesized, and 1,3-bis(4-acetamidophenyl)adamantane can be synthesized directly by alkali hydrolysis. Bis(4-phenylamine)adamantane. This synthetic route has the advantages of high reaction yield and easy purification, which greatly facilitates the synthesis of 1,3-adamantane diaryl derivatives.
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