(3S)-1,2,3,4-四氢异喹啉-3-羧酸 - Names and Identifiers
Name | ()-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
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Synonyms | H-TIC-OH H-Dl-Tic-Oh H-DL-TIC-OH 1,2,3,4-Tetrahydroisoquinoline-3Carboxylic rac 3-Carboxy-1,2,3,4-tetrahydroisoquinoline 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid 3-Isoquinolinecarboxylicacid, 1,2,3,4-tetrahydro- 3-Isoquinolinecarboxylic acid, 1,2,3,4-tetrahydro- ()-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid DL-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID rac 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (RS)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid
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CAS | 67123-97-1 35186-99-3
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EINECS | 266-580-4 |
InChI | InChI=1/C10H11NO2/c12-10(13)9-5-7-3-1-2-4-8(7)6-11-9/h1-4,9,11H,5-6H2,(H,12,13) |
(3S)-1,2,3,4-四氢异喹啉-3-羧酸 - Physico-chemical Properties
Molecular Formula | C10H11NO2
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Molar Mass | 177.2 |
Density | 1.225±0.06 g/cm3(Predicted) |
Melting Point | 358°C |
Boling Point | 372.0±42.0 °C(Predicted) |
Solubility | Sodium Hydroxide, Water |
Appearance | Solid |
Color | White |
pKa | 2.21±0.20(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,2-8°C |
(3S)-1,2,3,4-四氢异喹啉-3-羧酸 - Risk and Safety
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin.
R22 - Harmful if swallowed
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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.
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(3S)-1,2,3,4-四氢异喹啉-3-羧酸 - Introduction
()-1,2,3, acid is an organic compound with the molecular formula C10H11NO2. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: (-1,2,3), acid is colorless crystal.
-Solubility: It has low solubility in water and is soluble in some organic solvents such as alcohols and ketones.
-Acid and alkaline: It is a carboxylic acid that can react with alkali to form a salt.
Use:
-Drug intermediates:()-1,2,3, acid is often used as an intermediate for the synthesis of various drugs, especially for the synthesis of quinolone antibiotics.
-Scientific research: It can be used in the field of scientific research, such as the synthesis of organic compounds and drug research.
Preparation Method:
-There are many synthesis methods, but a common method is to react terephthalic acid with alkylamine or arylamine under acidic conditions, undergo dehydration cyclization reaction to obtain 1,2,3,4-tetrahydroisoquinoline derivatives, and then undergo oxidation reaction to obtain ()-1,2, 3,5 acid.
Safety Information:
-Since (-1,2,3), acid is an organic compound, care should be taken to comply with general safety procedures for chemicals when used, such as wearing appropriate personal protective equipment (such as gloves, protective glasses, etc.) and confirming that the laboratory is well ventilated.
-It may cause irritation and sensitivity to the human body, so direct contact with skin and eyes should be avoided when contacting. In case of contact, rinse with plenty of water and seek medical help.
-During storage and handling, the compound should be kept in a sealed container, away from high temperature, fire and oxidizing agents.
Last Update:2024-04-09 21:04:16