-Adamantyl alcohol
1-Hydroxyadamantane
CAS: 768-95-6
Molecular Formula: C10H16O
-Adamantyl alcohol - Names and Identifiers
| Name | 1-Hydroxyadamantane |
| Synonyms | 1-AD-OH 1-ADA-OH 1-Adamantol damantol-(1) 1-Adamatanol 1-ADAMANTANOL 1-Adamantanol 1-Diamond alkanol -Adamantyl alcohol 1-HYDROXYADAMANTANE 1-HYDROXYDIAMANTANE 1-Hydroxyadamantane TRICYCLO[3.3.1.1]DECAN-1-OL Tricyclo[3.3.1.1(3,7)]decan-1-ol TRICYCLO[3.3.1.1(3,7)]DECAN-1-OL tricyclo[3.3.1.1~3,7~]decan-1-ol tricyclo(3.3.1.1(sup3,7))decan-1-ol |
| CAS | 768-95-6 |
| EINECS | 212-202-8 |
| InChI | InChI=1/C10H16O/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9,11H,1-6H2 |
| InChIKey | VLLNJDMHDJRNFK-UHFFFAOYSA-N |
-Adamantyl alcohol - Physico-chemical Properties
| Molecular Formula | C10H16O |
| Molar Mass | 152.23 |
| Density | 0.8544 (rough estimate) |
| Melting Point | 247 °C (subl.) (lit.) |
| Boling Point | 214.73°C (rough estimate) |
| Flash Point | 240°C |
| Water Solubility | Soluble in ethanol , methanol, and diethyl ether. Partly miscible in water. |
| Solubility | Chloroform (Sparingly), Methanol (Slightly) |
| Vapor Presure | 0.00466mmHg at 25°C |
| Appearance | White powder |
| Color | White to off-white |
| BRN | 1903952 |
| pKa | 15.38±0.20(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.4880 (estimate) |
| MDL | MFCD00074729 |
| Use | As an intermediate for the synthesis of adamantanes |
-Adamantyl alcohol - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S36 - Wear suitable protective clothing. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
| WGK Germany | 3 |
| RTECS | AU4980000 |
| HS Code | 29061900 |
| Hazard Note | Irritant |
-Adamantyl alcohol - Reference Information
| Overview | 1-adamantanol (English 1-Adamantanol) is also called 1-hydrooxyadamantane, 1-tricyclo [3.3.1.1(3.7)] Decyl alcohol, white crystalline powder at room temperature, melting point> 240 ℃, soluble in organic solvents, insoluble in water, and sublimable. Used in the manufacture of synthetic adamantane derivatives and adabalin. 1-adamantane acetic acid can be obtained by reacting with vinylidene chloride. 1-adamantane acetic acid is further brominated, 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, which can directly synthesize 1,3-bis (4-acetylaminophenyl) adamantane, and synthesize 1,3-bis (4-aniline) adamantane by alkaline hydrolysis. This synthesis route has the advantages of high reaction yield and easy purification, which greatly facilitates 1, synthesis of 3-adamantane diaryl derivatives. |
| Uses | 1-adamantanol is used as an intermediate for the synthesis of adamantanes. Used in the manufacture of synthetic adamantane derivatives and adabalin. 1-adamantane acetic acid can be obtained by reacting with vinylidene chloride. |
| NIST chemical information | Information provided by: webbook.nist.gov (external link) |
Last Update：2024-04-09 21:04:16
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View History
-Adamantyl alcohol
1,3,3,5-Pentanetetracarboxylicacid, 1,3,3,5-tetraethyl ester
ethyl 2-morpholino-6-phenyl-4-(trifluoromethyl)-4H-1,3,5-oxadiazine-4-carboxylate
1,3,3,5-Pentanetetracarboxylicacid, 1,3,3,5-tetraethyl ester
ethyl 2-morpholino-6-phenyl-4-(trifluoromethyl)-4H-1,3,5-oxadiazine-4-carboxylate