(2-(Benzyloxy)phenyl)methanamine

Base Information

Chemical Name:(2-(Benzyloxy)phenyl)methanamine
CAS No.:108289-24-3
Molecular Formula:C₁₄H₁₅NO
Molecular Weight:213.279
Hs Code.:2922390090
DSSTox Substance ID:DTXSID80548470
Wikidata:Q82427182
Mol file:108289-24-3.mol

Synonyms:(2-(Benzyloxy)phenyl)methanamine;108289-24-3;2-BENZYLOXYBENZYLAMINE;(2-phenylmethoxyphenyl)methanamine;1-[2-(benzyloxy)phenyl]methanamine;[2-(BENZYLOXY)PHENYL]METHANAMINE;2-Benzyloxy-benzylamine;o-benzyloxybenzylamine;SCHEMBL2568609;DTXSID80548470;KOGOOCNDBVXUPW-UHFFFAOYSA-N;MFCD07786678;AKOS000126707;FS-4748;SB77279;AM807467;CS-0440551;EN300-58221;AB00999087-01

Suppliers and Price of (2-(Benzyloxy)phenyl)methanamine

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

Usbiological
2-Benzyloxybenzylamine
100mg
$ 305.00

TRC
2-Benzyloxybenzylamine
250mg
$ 75.00

TRC
2-Benzyloxybenzylamine
100mg
$ 45.00

Oakwood
(2-(Benzyloxy)phenyl)methanamine 95+%
1g
$ 186.00

Labseeker
2-Benzyloxybenzylamine 98
100g
$ 3208.00

Labseeker
2-Benzyloxybenzylamine 98
50g
$ 2292.00

Labseeker
2-Benzyloxybenzylamine 98
25g
$ 1550.00

Crysdot
(2-(Benzyloxy)phenyl)methanamine 97%
10g
$ 600.00

Crysdot
(2-(Benzyloxy)phenyl)methanamine 97%
5g
$ 400.00

Atlantic Research Chemicals
1-[2-(Benzyloxy)phenyl]methanamine 95%
1gm:
$ 159.06

Total 20 raw suppliers

Chemical Property of (2-(Benzyloxy)phenyl)methanamine

Chemical Property:

PSA：35.25000
LogP:3.42460
Storage Temp.:2-8°C
XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:213.115364102
Heavy Atom Count:16
Complexity:189

Purity/Quality:

97% ^*data from raw suppliers

2-Benzyloxybenzylamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC2=CC=CC=C2CN
Uses 2-Benzyloxybenzylamine is used as a reactant in the preparation of dihydrobenzoxazepinone derivatives via Ugi reaction and intramolecular Mitsunobu cyclization.

Technology Process of (2-(Benzyloxy)phenyl)methanamine

There total 7 articles about (2-(Benzyloxy)phenyl)methanamine 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: 71.0%

: 74511-44-7
o-(benzyloxy)benzonitrile

: 108289-24-3
(2-(benzyloxy)phenyl)methanamine

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 66 ℃; for 5h;
DOI:10.1002/ejoc.201900263

Reference yield:

: 2-(benzyloxy)benzaldehyde oxime

: 108289-24-3
(2-(benzyloxy)phenyl)methanamine

Guidance literature:: With acetic acid; zinc; at 60 - 70 ℃; for 1h;
DOI:10.1016/j.ejmech.2017.04.019

Reference yield:

: 100-39-0
benzyl bromide

: 108289-24-3
(2-(benzyloxy)phenyl)methanamine

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 0.17 h

1.2: 4 h / 40 °C

2.1: hydroxylamine hydrochloride; sodium hydroxide / water; methanol / 1 h / 70 °C

3.1: acetic acid; zinc / 1 h / 60 - 70 °C

With hydroxylamine hydrochloride; potassium carbonate; acetic acid; sodium hydroxide; zinc; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2017.04.019