212312-33-9 - Names and Identifiers
| Name | (3aR,8aS)-2-[2-(diphenylphosphino)phenyl]-3a,8a-dihydro-8H-Indeno[1,2-d]oxazole
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| Synonyms | (R,S)-In-Phox
(3aR,8aS)-2[2-(diphenylphosphanyl)phenyl]-3a,8a-dihydroindane[1,2-d]oxazole
(3aR,8aS)-2-[2-(diphenylphosphino)phenyl]-3a,8a-dihydro-8H-Indeno[1,2-d]oxazole
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| CAS | 212312-33-9
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212312-33-9 - Physico-chemical Properties
| Molecular Formula | C28H22NOP
|
| Molar Mass | 419.45 |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
212312-33-9 - Introduction
(3aR,8aS)-2-[2-(diphenylphosphino)phenyl]-3a,8a-dihydro-8h-indeno [1,2-d]oxazole is an organic compound with the following properties:
Nature:
-Appearance: Usually white or light yellow crystal
-Solubility: Soluble in some organic solvents, such as chloroform, methanol and dimethyl sulfoxide
-Molecular weight: about 513.55g/mol
Use:
-This compound is commonly used as a chiral ligand, has good coordination properties, and can be used for metal-catalyzed reactions in organic synthesis reactions
-It can be used to synthesize organometallic compounds, such as transition metal complexes
-In the field of organic chemistry, it has a wide range of applications in asymmetric catalytic reactions and natural product synthesis
Method:
- (3aR,8aS)-2-[2-(diphenylphosphino)phenyl]-3a,8a-dihydro-8H-Indeno[1,2-d]oxazole can be synthesized by various methods, one of the commonly used methods is the synthesis of amides by N-oxide. First, the N-oxide is formed by the reaction, and then the target compound is formed by dehydration.
Safety Information:
-Due to the lack of relevant toxicity and safety test data, please take appropriate safety measures when conducting experiments or using this compound.
-It may be an irritating compound that may irritate the respiratory system, eyes and skin, so appropriate protective measures should be taken.
-When using and handling, you should abide by the laboratory's safe operating procedures, and follow relevant laws, regulations and guidelines.
Last Update：2024-04-09 21:01:54