3-benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylic Acid

Base Information

Chemical Name:3-benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylic Acid
CAS No.:186376-32-9
Molecular Formula:C13H15NO2
Molecular Weight:217.26
Hs Code.:2933990090
DSSTox Substance ID:DTXSID20450482
Mol file:186376-32-9.mol

Synonyms:3-benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylic Acid;186376-32-9;exo-3-Benzyl-3-azabicyclo-[3.1.0]hexane-6-carboxylicacid;SCHEMBL8919911;DTXSID20450482;YGNSZJXUFXZCPP-UHFFFAOYSA-N;PB24334;CS-0055235;A850287;3-benzyl-3-aza-bicyclo[3.1.0]hexane-6-carboxylic acid

Suppliers and Price of 3-benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylic Acid

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

Crysdot
3-Benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylicacid 95+%
1g
$ 540.00

Chemenu
3-benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylicacid 95%
1g
$ 505.00

American Custom Chemicals Corporation
3-BENZYL-3-AZABICYCLO[3.1.0]HEXANE-6-CARBOXYLIC ACID 95.00%
5MG
$ 505.69

Alichem
3-Benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylicacid
1g
$ 902.58

Total 5 raw suppliers

Chemical Property of 3-benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylic Acid

Chemical Property:

PSA：40.54000
LogP:1.38690
Storage Temp.:2-8°C
XLogP3:-0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:217.110278721
Heavy Atom Count:16
Complexity:274

Purity/Quality:

97% ^*data from raw suppliers

3-Benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylicacid 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C2C(C2C(=O)O)CN1CC3=CC=CC=C3

Technology Process of 3-benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylic Acid

There total 2 articles about 3-benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylic Acid 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: 57.0%

: (1R,5S,6r)-ethyl 3-benzyl-3-azabicyclo[3.1.0]hexane-6-carboxylate

: 186376-32-9,174456-80-5
(1α,5α,6α)-3-benzyl-3-azabicyclo [3.1.0]hexane-6-carboxylic acid

Guidance literature:: In aq. hydrochloric acid;

Reference yield:

: 134575-06-7,846024-42-8
ethyl (1α,5α,6α)-3-benzyl-3-azabicyclo[3.1.0]hexane-2,4-dione-6-carboxylate

: 186376-32-9,174456-80-5
(1α,5α,6α)-3-benzyl-3-azabicyclo [3.1.0]hexane-6-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium tetrahydroborate; boron trifluoride diethyl etherate / tetrahydrofuran / 0 °C

1.2: 8 h / 0 - 20 °C / Reflux

2.1: sodium hydroxide / 1,4-dioxane / 20 - 70 °C

With sodium tetrahydroborate; boron trifluoride diethyl etherate; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane;