(3-Benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol

Base Information

Chemical Name:(3-Benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol
CAS No.:871727-08-1
Molecular Formula:C13H17NO
Molecular Weight:203.284
Hs Code.:
DSSTox Substance ID:DTXSID60602307

Synonyms:(3-Benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol;871727-08-1;{3-BENZYL-3-AZABICYCLO[3.1.0]HEXAN-6-YL}METHANOL;MFCD16140332;SCHEMBL1010709;DTXSID60602307;NMJRXNUMGKZPHG-UHFFFAOYSA-N;PB33264;SY097151;DB-200201;CS-0137454;F30480;(3-Benzyl-3-azabicyclo[3.1.0]hex-6-yl)methanol;A806802;(3-benzyl-3-azabicyclo[3.1.0]hex-6-yl) methanol;(3-Benzyl-3-aza-bicyclo[3.1.0]hexan-6-yl)methanol;(3-benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol;((1R,5S,6R)-3-Benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol

Suppliers and Price of (3-Benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol

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]hexan-6-yl)methanol 97%
5g
$ 2187.00

Crysdot
(3-Benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol 97%
1g
$ 727.00

Total 3 raw suppliers

Chemical Property of (3-Benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol

Chemical Property:

PSA：23.47000
LogP:1.29460
XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:203.131014166
Heavy Atom Count:15
Complexity:213

Purity/Quality:

NLT 98% ^*data from raw suppliers

(3-Benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C2C(C2CO)CN1CC3=CC=CC=C3

Technology Process of (3-Benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol

There total 3 articles about (3-Benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol 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: 51.0%

: 146726-13-8,846024-42-8
3-benzyl-3-azabicyclo[3.1.0]hexane-2,4-dione-6-carboxylic acid ethyl ester

: 871727-08-1
(3-benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol

Guidance literature:: 3-benzyl-3-azabicyclo[3.1.0]hexane-2,4-dione-6-carboxylic acid ethyl ester; With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 60 ℃; for 36h;

With water; ammonium chloride; In tetrahydrofuran; at 0 ℃;

Reference yield:

: 134575-05-6
ethyl 5-benzyl-4,6-dioxo-1,3a,4,5,6,6a-hexahydropyrrolo[3,4-c]pyrazole-3-carboxylate

: 871727-08-1
(3-benzyl-3-azabicyclo[3.1.0]hexan-6-yl)methanol

Guidance literature:: Multi-step reaction with 2 steps

1: 1 h / 190 °C

2: lithium aluminium tetrahydride / tetrahydrofuran / 16 h / 0 °C / Inert atmosphere; Reflux

With lithium aluminium tetrahydride; In tetrahydrofuran;