1147557-68-3

1147557-68-3 - Names and Identifiers

Name	tert-Butyl 9-hydroxy-3-oxa-7-azabicyclo[3.3.1]nonane-7-carboxylate
Synonyms	7-Boc-3-oxa-7-azabicyclo[3.3.1]nonan-9-ol tert-Butyl 9-hydroxy-3-oxa-7-azabicyclo[3.3.1]nonane-7-carbo... tert-Butyl 9-hydroxy-3-oxa-7-azabicyclo[3.3.1]nonane-7-carboxylate tert-Butyl (1R,5S)-9-hydroxy-3-oxa-7-azabicyclo[3.3.1]nonane-7-carboxylate Tert-Butyl 9-Hydroxy-3-Oxa-7-Azabicyclo[3.3.1]Nonane-7-Carboxylate(WX125246) 9-HYDROXY-3-OXA-7-AZABICYCLO[ 3.3.1]NONANE-7- CARBOXYLIC ACID TERT-BUTYLESTER 3-Oxa-7-azabicyclo[3.3.1]nonane-7-carboxylic acid, 9-hydroxy-, 1,1-dimethylethyl ester
CAS	1147557-68-3

1147557-68-3 - Physico-chemical Properties

Molecular Formula	C12H21NO4
Molar Mass	243.3
Storage Condition	2-8℃

1147557-68-3 - Introduction

7-tert-butoxycarbonyl-3-oxa-7-azabicyclo [3,3,1] nonan-9-ol, often referred to as TETEROL, its properties, uses, preparation and safety information are as follows:

Nature:
-Appearance: White solid
-Molecular formula: C13H25NO3
-Molecular weight: 247.35g/mol
-Melting point: 110-112°C
-Stability: stable, not easy to decompose

Use:
- TETEROL are commonly used as synthetic intermediates for polar solvents, surfactants and ionic liquids.
-It can also be used as a chemical reagent and a catalyst in certain organic syntheses.

Method:
-The preparation of TETEROL is generally obtained by oxygen hybridization and nitrogen hybridization reactions.
-The specific method is to react an appropriate amount of substrate with a catalyst under suitable conditions to generate a TETEROL product.

Safety Information:
- TETEROL are chemicals and have certain hazards. Please strictly abide by the safety operation procedures and wear protective clothing, gloves and glasses during operation.
-Avoid inhaling gases, fumes or vapors, and avoid contact with skin and eyes.
-In case of accidental contact, immediately flush the affected area with plenty of water and seek medical help.
-Keep away from ignition and heat sources when storing and handling.

Last Update：2024-04-10 22:29:15