5-(Benzylaminomethyl)-2-methoxyphenol

Base Information

Chemical Name:5-(Benzylaminomethyl)-2-methoxyphenol
CAS No.:58451-94-8
Molecular Formula:C15H17NO2
Molecular Weight:243.3
Hs Code.:2922509090
DSSTox Substance ID:DTXSID20373440
Wikidata:Q82161606
Mol file:58451-94-8.mol

Synonyms:5-(Benzylaminomethyl)-2-methoxyphenol;58451-94-8;5-[(benzylamino)methyl]-2-methoxyphenol;5-((Benzylamino)methyl)-2-methoxyphenol;DTXSID20373440;AKOS000226072;SB80973;5-(benzylamino-methyl)-2-methoxy-phenol;5-(benzylaminomethyl)-2-methoxyphenol, AldrichCPR

Suppliers and Price of 5-(Benzylaminomethyl)-2-methoxyphenol

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
5-((Benzylamino)methyl)-2-methoxyphenol 97%
1g
$ 546.00

American Custom Chemicals Corporation
5-(BENZYLAMINOMETHYL)-2-METHOXYPHENOL 98.00%
1G
$ 1149.23

AHH
5-(Benzylaminomethyl)-2-methoxyphenol 98%
1g
$ 260.00

Total 13 raw suppliers

Chemical Property of 5-(Benzylaminomethyl)-2-methoxyphenol

Chemical Property:

PSA：41.49000
LogP:3.08150
XLogP3:2.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:243.125928785
Heavy Atom Count:18
Complexity:229

Purity/Quality:

98%min ^*data from raw suppliers

5-((Benzylamino)methyl)-2-methoxyphenol 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xn
Statements: 22

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C=C(C=C1)CNCC2=CC=CC=C2)O

Technology Process of 5-(Benzylaminomethyl)-2-methoxyphenol

There total 1 articles about 5-(Benzylaminomethyl)-2-methoxyphenol 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:

: 621-59-0
isovanillin

: 100-46-9
benzylamine

: 58451-94-8
N-(3-Hydroxy-4-methoxybenzyl)benzylamin

Guidance literature:: Multistep reaction; (i) Et₃N, EtOH, (ii) H₂, Pd-C;
DOI:10.1248/cpb.23.3101

Reference yield: 60.0%

: carbonic acid (E)-4-bromobut-2-en-1-yl methyl ester

: 58451-94-8
N-(3-Hydroxy-4-methoxybenzyl)benzylamin

: 1374156-32-7
C₂₁H₂₅NO₅

Guidance literature:: With triethylamine; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/ol3008793

Reference yield:

: 58451-94-8
N-(3-Hydroxy-4-methoxybenzyl)benzylamin

: 1374156-61-2
C₁₉H₂₁NO₂

: 1374156-51-0
C₁₉H₂₁NO₂

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

2: dmap; bis(1,5-cyclooctadiene)diiridium(I) dichloride; (3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)-bis-(1-phenyl-ethyl)-amine / tetrahydrofuran / 20 °C / Inert atmosphere

With dmap; bis(1,5-cyclooctadiene)diiridium(I) dichloride; triethylamine; (3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)-bis-(1-phenyl-ethyl)-amine; In tetrahydrofuran; 2: Friedel Crafts alkylation;
DOI:10.1021/ol3008793