N-[(4-Amino-3,5-dimethylphenyl)methyl]-2,4,6-trimethylaniline

Base Information

Chemical Name:N-[(4-Amino-3,5-dimethylphenyl)methyl]-2,4,6-trimethylaniline
CAS No.:89210-27-5
Molecular Formula:C18H24N2
Molecular Weight:268.402
Hs Code.:
DSSTox Substance ID:DTXSID30533073
Wikidata:Q82406144

Synonyms:89210-27-5;DTXSID30533073;N-[(4-Amino-3,5-dimethylphenyl)methyl]-2,4,6-trimethylaniline

Suppliers and Price of N-[(4-Amino-3,5-dimethylphenyl)methyl]-2,4,6-trimethylaniline

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-[(4-Amino-3,5-dimethylphenyl)methyl]-2,4,6-trimethylaniline

Chemical Property:

XLogP3:4.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:268.193948774
Heavy Atom Count:20
Complexity:280

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C(C(=C1)C)NCC2=CC(=C(C(=C2)C)N)C)C

Technology Process of N-[(4-Amino-3,5-dimethylphenyl)methyl]-2,4,6-trimethylaniline

There total 6 articles about N-[(4-Amino-3,5-dimethylphenyl)methyl]-2,4,6-trimethylaniline 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:

: 910614-10-7
(3,5-Dimethyl-4-nitro-benzyl)-(2,4,6-trimethyl-phenyl)-amine

: 89210-27-5
N-(4-amino-3,5-dimethylbenzyl)-2,4,6-trimethylbenzenamine

Guidance literature:: With sodium hydroxide; zinc; In ethanol; water; for 1h; Heating;
DOI:10.1021/jo00183a024

Reference yield:

: 18515-22-5
(3,5-dimethyl-4-nitrophenyl)methanol

: 89210-27-5
N-(4-amino-3,5-dimethylbenzyl)-2,4,6-trimethylbenzenamine

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / ceric ammonium nitrate / acetic acid / 0.5 h / Heating

2: 85 percent / formic acid (90percent), acetic anhydride / 3 h / Heating

3: NaOH, zinc dust / H₂O; ethanol / 1 h / Heating

With sodium hydroxide; formic acid; ammonium cerium(IV) nitrate; acetic anhydride; zinc; In ethanol; water; acetic acid;
DOI:10.1021/jo00183a024

Reference yield:

: 603-71-4,34505-32-3,82795-90-2
nitromesitylene

: 89210-27-5
N-(4-amino-3,5-dimethylbenzyl)-2,4,6-trimethylbenzenamine

Guidance literature:: Multi-step reaction with 5 steps

1: 19.5 g / CrO₃ / acetic acid / 2 h

2: 75 percent / NaBH₄, BF₃ etherate / tetrahydrofuran

3: 90 percent / ceric ammonium nitrate / acetic acid / 0.5 h / Heating

4: 85 percent / formic acid (90percent), acetic anhydride / 3 h / Heating

5: NaOH, zinc dust / H₂O; ethanol / 1 h / Heating

With chromium(VI) oxide; sodium hydroxide; sodium tetrahydroborate; formic acid; ammonium cerium(IV) nitrate; boron trifluoride diethyl etherate; acetic anhydride; zinc; In tetrahydrofuran; ethanol; water; acetic acid;
DOI:10.1021/jo00183a024