Fmoc-2-aminobicyclo[2.2.1]heptane-2-carboxylic acid (mixture of isomers)

Base Information

Chemical Name:Fmoc-2-aminobicyclo[2.2.1]heptane-2-carboxylic acid (mixture of isomers)
CAS No.:188751-57-7
Molecular Formula:C23H23NO4
Molecular Weight:377.44
Hs Code.:
Mol file:188751-57-7.mol

Synonyms:

Suppliers and Price of Fmoc-2-aminobicyclo[2.2.1]heptane-2-carboxylic acid (mixture of isomers)

Supply Marketing:

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

Matrix Scientific
Fmoc-2-aminobicyclo[2.2.1]heptane-2-carboxylicacid (mixture of isomers)
1g
$ 895.00

Matrix Scientific
Fmoc-2-aminobicyclo[2.2.1]heptane-2-carboxylicacid (mixture of isomers)
100mg
$ 179.00

Total 2 raw suppliers

Chemical Property of Fmoc-2-aminobicyclo[2.2.1]heptane-2-carboxylic acid (mixture of isomers)

Chemical Property:

Boiling Point:600.0±29.0 °C(Predicted)
PKA:4.00±0.20(Predicted)
PSA：75.63000
Density:1.35±0.1 g/cm3(Predicted)
LogP:4.55940

Purity/Quality:

98%min ^*data from raw suppliers

Fmoc-2-aminobicyclo[2.2.1]heptane-2-carboxylicacid (mixture of isomers) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Fmoc-2-aminobicyclo[2.2.1]heptane-2-carboxylic acid (mixture of isomers)

There total 3 articles about Fmoc-2-aminobicyclo[2.2.1]heptane-2-carboxylic acid (mixture of isomers) 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: 21.0%

: 82911-69-1
N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide

: 20448-79-7,33889-51-9,33889-53-1,33889-52-0
2-aminonorbornane-2-carboxylic acid

: 188751-57-7
2-(((9H-fluoren-9-yl)methoxy)carbonylamino)bicyclo[2.2.1]heptane-2-carboxylic acid

Guidance literature:: 2-aminonorbornane-2-carboxylic acid; With hydrogenchloride; In water; pH=10;

N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide; In water; acetonitrile; at 20 ℃;

Reference yield:

: 497-38-1
Norbornan-2-on

: 188751-57-7
2-(((9H-fluoren-9-yl)methoxy)carbonylamino)bicyclo[2.2.1]heptane-2-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: water / ethanol / 12 h / 50 °C

2.1: sodium hydroxide; ethanol / Reflux

3.1: hydrogenchloride / water / pH 10

3.2: 20 °C

With hydrogenchloride; ethanol; water; sodium hydroxide; In ethanol; water;

Reference yield:

: 22264-49-9
spiro[bicyclo[2.2.1]heptane-2',5'-imidazolidine[2,4]dione]

: 188751-57-7
2-(((9H-fluoren-9-yl)methoxy)carbonylamino)bicyclo[2.2.1]heptane-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydroxide; ethanol / Reflux

2.1: hydrogenchloride / water / pH 10

2.2: 20 °C

With hydrogenchloride; ethanol; sodium hydroxide; In water;