Tert-butyl (4-amino-4-phenylbutyl)carbamate

Base Information

Chemical Name:Tert-butyl (4-amino-4-phenylbutyl)carbamate
CAS No.:357443-58-4
Molecular Formula:C₁₅H₂₄N₂O₂
Molecular Weight:264.368
Hs Code.:
European Community (EC) Number:845-796-8
Mol file:357443-58-4.mol

Synonyms:357443-58-4;tert-butyl N-(4-amino-4-phenylbutyl)carbamate;TERT-BUTYL (4-AMINO-4-PHENYLBUTYL)CARBAMATE;TERT-BUTYL 4-AMINO-4-PHENYLBUTYLCARBAMATE;SCHEMBL10323702;IHZJZEXHKLIMKX-UHFFFAOYSA-N;MFCD09741892;AKOS000149761;AS-38713;DA-42645;t-Butyl (4-amino-4-phenylbutyl)carbamate;CS-0215055;EN300-217643;TERT-BUTYL(4-AMINO-4-PHENYLBUTYL)CARBAMATE;(4-amino-4-phenylbutyl)carbamic acid, 1,1-dimethylethyl ester

Suppliers and Price of Tert-butyl (4-amino-4-phenylbutyl)carbamate

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

Alichem
Tert-butyl(4-amino-4-phenylbutyl)carbamate
1g
$ 1022.67

Alichem
Tert-butyl(4-amino-4-phenylbutyl)carbamate
250mg
$ 450.17

AK Scientific
Tert-butyl(4-amino-4-phenylbutyl)carbamate
10g
$ 4492.00

Total 3 raw suppliers

Chemical Property of Tert-butyl (4-amino-4-phenylbutyl)carbamate

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:264.183778013
Heavy Atom Count:19
Complexity:268

Purity/Quality:

98% ^*data from raw suppliers

Tert-butyl(4-amino-4-phenylbutyl)carbamate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NCCCC(C1=CC=CC=C1)N
Uses tert-Butyl N-(4-amino-4-phenylbutyl)carbamate is used in the preparation of cyclic benzamidines as NR2B-selective NMDA receptor antagonists which may be used in analgesic formulations.

Technology Process of Tert-butyl (4-amino-4-phenylbutyl)carbamate

There total 8 articles about Tert-butyl (4-amino-4-phenylbutyl)carbamate 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:

: (E)-tert-butyl 4-(hydroxyimino)-4-phenylbutylcarbamate

: 357443-58-4
(4-Amino-4-phenylbutyl)carbamic acid, 1,1-dimethylethyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol;
DOI:10.1016/j.bmcl.2007.04.084

Reference yield:

: [4-(Hydroxyimino)-4-phenylbutyl]carbamic acid, 1,1-dimethylethyl ester

: 357443-58-4
(4-Amino-4-phenylbutyl)carbamic acid, 1,1-dimethylethyl ester

Guidance literature:: palladium on charcoal; In ethanol;

Reference yield:

: C₁₀H₁₂N₄O

: 357443-58-4
(4-Amino-4-phenylbutyl)carbamic acid, 1,1-dimethylethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd/C / ethanol

2: H₂ / Pd/C / methanol

With hydrogen; palladium on activated charcoal; In methanol; ethanol;
DOI:10.1016/j.bmcl.2007.04.084