10,11 - dihidrógeno - 5H - dibenzo [b, f] azaping - 3 - Amina CAS 10464 - 35 - 4

10,11-dihydro-5H-dibenzo[b,f]azepin-3-amine - Names and Identifiers

Nombre	10,11-dihydro-5H-dibenzo[b,f]azepin-3-amine
Sinónimos	10,11-Dihydro-5H-dibenz[B,F]azepin-3-amine 10,11-dihydro-5H-dibenzo[b,f]azepin-3-amine 10,11-Dihydro-5H-dibenzo[b,f]azepin-3-aMine 5H-Dibenz[b,f]azepin-3-amine, 10,11-dihydro- 6,11-dihydro-5H-benzo[b][1]benzazepin-2-amine
CAS	10464-35-4

10,11-dihydro-5H-dibenzo[b,f]azepin-3-amine - Physico-chemical Properties

Fórmula Molecular	C14H14N2
Masa Molar	210.27
Densidad	1.154±0.06 g/cm3(Predicted)
Punto de fusión	98-100 °C
punto Boling	386.3±42.0 °C(Predicted)
PKa	5.14±0.20(Predicted)

10,11-dihydro-5H-dibenzo[b,f]azepin-3-amine - Introduction

3-amino -10, 11-dihydrobenzo [B, f] azepine (abbreviated as BFNHZ) is a compound with a heterocyclic structure. The following is some information about the properties, uses, methods and safety of the BFNHZ:

Naturaleza:
-Appearance: BFNHZ is a yellow to orange solid
-Solubility: It can be dissolved in organic solvents, such as dimethyl sulfoxide, dichloromethane and ether
-Melting point: The melting point of BFNHZ is about 220-230 degrees Celsius

Uso:
-Optoelectronic devices: BFNHZ has good electronic transmission performance and light absorption characteristics, and can be used in the field of organic optoelectronic devices, such as organic solar cells and organic light-emitting diodes (OLED)
-Dye: BFNHZ can also be used as a dye synthesis intermediate, used in the synthesis of dyes and as a photosensitizer in dye-sensitized solar cells

Método de preparación:
-The preparation of BFNHZ usually involves several steps of organic synthesis. One of the most commonly used methods is the synthesis of BFNHZ by electrophilic substitution and nitration reactions and reduction reactions.

Información de seguridad:
- BFNHZ is considered a relatively safe compound under normal conditions of use. However, due to its fluctuation and protection group, appropriate protective measures should be taken during its handling and operation, such as wearing gloves, eye and respiratory protection devices. In addition, the experiment should be conducted in a well-ventilated area, avoiding contact with the mouth, eyes and skin. In case of accidental contact, rinse immediately with plenty of water and seek medical help.