119102-90-8
7-Benzyl-2-oxa-7-AZA-SPIRO[4.4]nonan-1-one
CAS: 119102-90-8
Molecular Formula: C14H17NO2
119102-90-8 - Names and Identifiers
| Name | 7-Benzyl-2-oxa-7-AZA-SPIRO[4.4]nonan-1-one |
| Synonyms | 7-Benzyl-2-oxa-7-azaspiro[4.4]nonan-1-on 7-benzyl-1-oxa-7-azaspiro[4.4]nonan-2-one 7-BENZYL-2-OXA-7-AZA-SPIRO[4.4]NONAN-1-ONE 7-Benzyl-2-oxa-7-AZA-SPIRO[4.4]nonan-1-one 2-oxa-7-azaspiro[4.4]nonan-1-one, 7-(phenylmethyl)- 2-Oxa-7-azaspiro[4.4]nonan-1-one, 7-(phenylMethyl)- |
| CAS | 119102-90-8 |
| InChI | InChI=1/C14H17NO2/c16-13-14(7-9-17-13)6-8-15(11-14)10-12-4-2-1-3-5-12/h1-5H,6-11H2 |
119102-90-8 - Physico-chemical Properties
| Molecular Formula | C14H17NO2 |
| Molar Mass | 231.29 |
| Density | 1.19g/cm3 |
| Boling Point | 391.5°C at 760 mmHg |
| Flash Point | 154.8°C |
| Vapor Presure | 2.46E-06mmHg at 25°C |
| Storage Condition | 2-8°C |
| Refractive Index | 1.589 |
119102-90-8 - Introduction
7-benzyl -1-oxa -7-azaspiro [4,4]-2-nonanone is an organic compound, the chemical formula is C17H21NO, it is a photosensitive and thermosensitive heterocyclic compounds. The compound has a special structure, which contains a spiro ring structure and a thiol functional group.
The main use of the compound is as a photochromic material, and it has a wide range of applications in photosensitive magic photo paper, photosensitive electroplating, photosensitive film, etc.
There are two main methods for preparing 7-benzyl -1-oxa -7-azaspiro [4,4]-2-nonanone. One is through the reaction synthesis of thiol functional groups, such as the reaction of thiol alcohol and sodium nitrite, and then with benzyl bromide compounds to produce the target product. The other is through the synthesis of oxazole ring, and then react with benzyl bromide compound to generate the target product. The preparation process requires special laboratory facilities and suitable reaction conditions.
Regarding safety information, there are currently no clear toxicity data and safety evaluation for 7-benzyl-1-oxa-7-azaspiro [4,4]-2-nonanone. However, as an organic compound, it must be handled under laboratory conditions and appropriate protective measures must be taken to avoid contact with skin, eyes and inhalation. When using this compound, care should be taken to prevent it from reacting with strong oxidants and flammable substances, and to properly store and dispose of waste. Before using this compound, it is recommended to conduct a safety assessment and refer to relevant safety data.
The main use of the compound is as a photochromic material, and it has a wide range of applications in photosensitive magic photo paper, photosensitive electroplating, photosensitive film, etc.
There are two main methods for preparing 7-benzyl -1-oxa -7-azaspiro [4,4]-2-nonanone. One is through the reaction synthesis of thiol functional groups, such as the reaction of thiol alcohol and sodium nitrite, and then with benzyl bromide compounds to produce the target product. The other is through the synthesis of oxazole ring, and then react with benzyl bromide compound to generate the target product. The preparation process requires special laboratory facilities and suitable reaction conditions.
Regarding safety information, there are currently no clear toxicity data and safety evaluation for 7-benzyl-1-oxa-7-azaspiro [4,4]-2-nonanone. However, as an organic compound, it must be handled under laboratory conditions and appropriate protective measures must be taken to avoid contact with skin, eyes and inhalation. When using this compound, care should be taken to prevent it from reacting with strong oxidants and flammable substances, and to properly store and dispose of waste. Before using this compound, it is recommended to conduct a safety assessment and refer to relevant safety data.
Last Update：2024-04-10 22:29:15
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CAS: 119102-90-8
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