34859-74-0
3-Chloroadamantane-1-carboxylic acid
CAS: 34859-74-0
Molecular Formula: C11H15ClO2
34859-74-0 - Names and Identifiers
| Name | 3-Chloroadamantane-1-carboxylic acid |
| Synonyms | BRN 2103172 AKOS BB-9607 IFLAB-BB F1928-0004 1-chloro-3-adamantanecarboxylicaci 3-CHLOROADAMANTANE CARBOXYLIC ACID 3-Chloroadamantane-1-carboxylic acid 3-CHLOROADAMANTANE-1-CARBOXYLIC ACID 1-Chloro-3-adamantanecarboxylic acid 3-Adamantanecarboxylic acid, 1-chloro- AVO3-Chloroadamantane-1-carboxylic Acid 3-chlorotricyclo[3.3.1.1~3,7~]decane-1-carboxylic acid tricyclo[3.3.1.1~3,7~]decane-1-carboxylic acid, 3-chloro- (5R,7R)-3-chlorotricyclo[3.3.1.1~3,7~]decane-1-carboxylate 3-Chlorotricyclo[3.3.1.1~3,7~]decane-1-carboxylic acid, 1-Carboxy-3-chloroadamantane |
| CAS | 34859-74-0 |
| InChI | InChI=1/C11H15ClO2/c12-11-4-7-1-8(5-11)3-10(2-7,6-11)9(13)14/h7-8H,1-6H2,(H,13,14)/p-1/t7-,8-,10?,11?/m1/s1 |
34859-74-0 - Physico-chemical Properties
| Molecular Formula | C11H15ClO2 |
| Molar Mass | 214.69 |
| Melting Point | 136 °C |
| Boling Point | 343.2°C at 760 mmHg |
| Flash Point | 161.4°C |
| Vapor Presure | 1.29E-05mmHg at 25°C |
| Storage Condition | 2-8°C |
| MDL | MFCD00167831 |
34859-74-0 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
| Hazard Class | IRRITANT |
34859-74-0 - Introduction
Acid is an organic compound with the chemical formula C11H15ClO2. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: Colorless solid
-melting point: 137-143 ℃
-Boiling point: not mentioned in references
Use:
Acid has certain uses in medicinal chemistry and organic synthesis, such as as raw materials for the synthesis of biologically active molecules and drug intermediates.
Preparation Method:
A common preparation method is to react 3-chloroadamantane-1-acetic acid with bromoacetic acid under alkaline conditions to obtain 3-chloroadamantane-1-acetic acid, which is then converted into 4-chloroadamantane-1-acetic acid by acid hydrolysis.
Safety Information:
-the acid is irritating to the skin, eyes and mucous membranes, and direct contact should be avoided.
-Wear appropriate protective gloves, glasses and breathing mask during use.
-Storage should be kept dry, sealed, and away from heat and flame.
-Appropriate laboratory instructions for safe handling and handling of waste need to be followed for use, storage and disposal.
Please note that the above information is for reference only. Specific experimental operations and safety measures should be evaluated and taken according to specific experimental conditions and requirements.
Nature:
-Appearance: Colorless solid
-melting point: 137-143 ℃
-Boiling point: not mentioned in references
Use:
Acid has certain uses in medicinal chemistry and organic synthesis, such as as raw materials for the synthesis of biologically active molecules and drug intermediates.
Preparation Method:
A common preparation method is to react 3-chloroadamantane-1-acetic acid with bromoacetic acid under alkaline conditions to obtain 3-chloroadamantane-1-acetic acid, which is then converted into 4-chloroadamantane-1-acetic acid by acid hydrolysis.
Safety Information:
-the acid is irritating to the skin, eyes and mucous membranes, and direct contact should be avoided.
-Wear appropriate protective gloves, glasses and breathing mask during use.
-Storage should be kept dry, sealed, and away from heat and flame.
-Appropriate laboratory instructions for safe handling and handling of waste need to be followed for use, storage and disposal.
Please note that the above information is for reference only. Specific experimental operations and safety measures should be evaluated and taken according to specific experimental conditions and requirements.
Last Update：2024-04-09 15:17:56
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CAS: 34859-74-0
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CAS: 34859-74-0
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View History
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