2-Azabicyclo[2.2.1]heptane

Base Information Edit

Chemical Name:2-Azabicyclo[2.2.1]heptane
CAS No.:279-24-3
Molecular Formula:C6H11N
Molecular Weight:97.16
Hs Code.:2933990090
Mol file:279-24-3.mol

Synonyms:2-Azanorbornane;

Suppliers and Price of 2-Azabicyclo[2.2.1]heptane

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
2-Azabicyclo[2.2.1]heptane
100mg
$ 85.00

SynQuest Laboratories
2-Azabicyclo[2.2.1]heptane 97%
250 mg
$ 160.00

SynQuest Laboratories
2-Azabicyclo[2.2.1]heptane 97%
1 g
$ 352.00

Matrix Scientific
2-Azabicyclo[2.2.1]heptane hydrochloride
500mg
$ 187.00

Matrix Scientific
2-Azabicyclo[2.2.1]heptane 97%
1g
$ 764.00

Matrix Scientific
2-Azabicyclo[2.2.1]heptane hydrochloride
1g
$ 287.00

Biosynth Carbosynth
2-Azabicyclo[2.2.1]heptane
250 mg
$ 150.00

Biosynth Carbosynth
2-Azabicyclo[2.2.1]heptane
100 mg
$ 75.00

Biosynth Carbosynth
2-Azabicyclo[2.2.1]heptane
50 mg
$ 50.00

Biosynth Carbosynth
2-Azabicyclo[2.2.1]heptane
500 mg
$ 250.00

Total 36 raw suppliers

Chemical Property of 2-Azabicyclo[2.2.1]heptane Edit

Chemical Property:

Vapor Pressure:5.169mmHg at 25°C
Melting Point:70-80 °C
Refractive Index:1.486
Boiling Point:144.1 °C at 760 mmHg
PKA:11.44±0.20(Predicted)
Flash Point:30.6 °C
PSA：12.03000
Density:0.96 g/cm³
LogP:1.88910
Storage Temp.:Keep in dark place,Inert atmosphere,Room temperature

Purity/Quality:

99% ^*data from raw suppliers

2-Azabicyclo[2.2.1]heptane ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn
Statements: 22-37/38-41-52
Safety Statements: 26-39

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-Azabicyclo[2.2.1]heptane

There total 5 articles about 2-Azabicyclo[2.2.1]heptane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 73.0%

: 24647-29-8
2-Azabicyclo[2.2.1]heptan-3-one

: 279-24-3
2-aza-bicyclo[2.2.1]heptane

Guidance literature:: 2-Azabicyclo[2.2.1]heptan-3-one; With bis(cyclopentadienyl)dihydrozirconium; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane; at 20 ℃; Glovebox; Inert atmosphere;

With hydrogenchloride; In diethyl ether; water; for 2h; Glovebox; Inert atmosphere;
DOI:10.1016/S1872-2067(21)63853-6

Reference yield:

: 542-92-7,25568-84-7,7313-32-8
cyclopenta-1,3-diene

: 279-24-3
2-aza-bicyclo[2.2.1]heptane

Guidance literature:: Multi-step reaction with 3 steps

1: 56 percent / 2) glac. acetic acid / CH₂Cl₂ / 1) 10 deg C, 3 h, 2) 20 deg C, 1 h

2: 97 percent / H₂ / 10percent Pd/C / ethyl acetate / 20 °C / 2625.2 Torr

3: 71 percent / LiAlH₄ / diethyl ether / 1) 20 deg C, 1 h, 2) reflux, 6 h

With lithium aluminium tetrahydride; hydrogen; acetic acid; palladium on activated charcoal; In diethyl ether; dichloromethane; ethyl acetate;

Reference yield:

: 49805-30-3
2-azabicyclo[2.2.1.]hept-5-en-3-one

: 279-24-3
2-aza-bicyclo[2.2.1]heptane

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / H₂ / 10percent Pd/C / ethyl acetate / 20 °C / 2625.2 Torr

2: 71 percent / LiAlH₄ / diethyl ether / 1) 20 deg C, 1 h, 2) reflux, 6 h

With lithium aluminium tetrahydride; hydrogen; palladium on activated charcoal; In diethyl ether; ethyl acetate;