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Home > products > Chemical Intermediates > MDL NO MFCD00074729 1-Adamantanol CAS 768-95-6

MDL NO MFCD00074729 1-Adamantanol CAS 768-95-6

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Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 768-95-6

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CAS 768-95-6 1-Adamantanol

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MDL NO MFCD00074729 1-Adamantanol

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
MDL NO MFCD00074729 1-Adamantanol CAS 768-95-6

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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