3-CBZ-3,6-DIAZABICYCLO[3.2.0]HEPTANE

3-CBZ-3,6-DIAZABICYCLO[3.2.0]HEPTANE - Names and Identifiers

Name	3-CBZ-3,6-DIAZABICYCLO[3.2.0]HEPTANE
Synonyms	3-CBZ-3,6-DIAZABICYCLO[3.2.0]HEPTANE benzyl 3,6-diazabicyclo[3.2.0]heptane-3-carboxylate 3,6-Diaza-bicyclo[3.2.0]heptane-3-carboxylic acid benzyl ester cis-3,6-Diazabicyclo[3.2.0]heptane-3-carboxylic acid benzyl ester 3,6-Diazabicyclo[3.2.0]heptane-3-carboxylicacid, phenylmethyl ester
CAS	370880-87-8
EINECS	604-604-1

3-CBZ-3,6-DIAZABICYCLO[3.2.0]HEPTANE - Physico-chemical Properties

Molecular Formula	C13H16N2O2
Molar Mass	232.278
Density	1.218±0.06 g/cm3(Predicted)
Boling Point	370.7±25.0 °C(Predicted)
pKa	10.70±0.20(Predicted)
Storage Condition	2-8℃

3-CBZ-3,6-DIAZABICYCLO[3.2.0]HEPTANE - Upstream Downstream Industry

Downstream Products

6-BOC-3,6-DIAZABICYCLO[3.2.0]HEPTANE

3-CBZ-3,6-DIAZABICYCLO[3.2.0]HEPTANE - Introduction

3-CBZ-3,6-DIAZABICYCLO[3.2.0]HEPTANE(3-CBZ-3,6-diazabicyclo[3.2.0]heptane) is an organic compound with some of the following properties:

1. Appearance: colorless to light yellow liquid.
2. Molecular formula: C12H16N2.
3. Molecular weight: 188.27g/mol.
4. Melting Point:-5 ℃.
5. Boiling point: 210-212 ℃.
6. Density: 0.976g/cm3.
7. Solubility: Soluble in most organic solvents.

3-CBZ-3,6-DIAZABICYCLO[3.2.0]HEPTANE is mainly used as a catalyst or intermediate in organic synthesis reactions. It has important application value in the synthesis of a variety of natural products, drugs and ionic liquids.

Method of preparing 3-CBZ-3,6-DIAZABICYCLO[3.2.0]HEPTANE:
A synthesis method is to react 1,4-cyclohexadiene with hydroquinone in the presence of an ammonia catalyst to generate 7, 8-dihydro-lh-cyclohexan [3.2.0] pyrrole, which is then reacted with benzoic anhydride to give 3-CBZ-3,6-DIAZABICYCLO[3.2.0]HEPTANE.

There is no public detailed data on the safety information of 3-CBZ-3,6-DIAZABICYCLO[3.2.0]HEPTANE. However, as an organic compound, care should be taken to use appropriate protective measures to avoid contact with skin, eyes and respiratory tract. It needs to be operated in a well-ventilated area and handled properly in a laboratory environment. In case of any unexpected situation or first aid situation, please immediately seek professional assistance.

Last Update：2024-04-09 21:54:55