Carbamic acid, (4-aminopentyl)-, 1,1-dimethylethyl ester (9CI)

Base Information

Chemical Name:Carbamic acid, (4-aminopentyl)-, 1,1-dimethylethyl ester (9CI)
CAS No.:701255-53-0
Molecular Formula:C₁₀H₂₂N₂O₂
Molecular Weight:202.297
Hs Code.:
Mol file:701255-53-0.mol

Synonyms:Carbamic acid, (4-aminopentyl)-, 1,1-dimethylethyl ester (9CI);CarbaMic acid, (4-aMinopentyl)-, 1,1-diMethylethyl ester;(4-Aminopentyl)carbamic acid tert-butyl ester

Suppliers and Price of Carbamic acid, (4-aminopentyl)-, 1,1-dimethylethyl ester (9CI)

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

TRC
1,1-Dimethylethyl(4-Aminopentyl)carbamate
10mg
$ 90.00

AK Scientific
Tert-butylN-(4-aminopentyl)carbamate
2.5g
$ 2291.00

Total 3 raw suppliers

Chemical Property of Carbamic acid, (4-aminopentyl)-, 1,1-dimethylethyl ester (9CI)

Chemical Property:

Boiling Point:303℃
Flash Point:137℃
Density:0.963

Purity/Quality:

98% ^*data from raw suppliers

1,1-Dimethylethyl(4-Aminopentyl)carbamate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Carbamic acid, (4-aminopentyl)-, 1,1-dimethylethyl ester (9CI)

There total 5 articles about Carbamic acid, (4-aminopentyl)-, 1,1-dimethylethyl ester (9CI) 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: 88.0%

: N⁴-benzyl N¹-t-butyl pent-2-ene-1,4-diyl(S,E)-dicarbamate

: 701255-53-0
t-butyl (S)-(4-aminopentyl)carbamate

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; Schlenk technique;
DOI:10.1039/d1ob01624e

Reference yield: 68.0%

: 591-77-5
1-methyl-1,4-butanediamine

: 6627-89-0
tert-butyl phenyl carbonate

: 701255-53-0
tert-butyl (4-aminopentyl)carbamate

Guidance literature:: In ethanol; at 90 ℃;
DOI:10.1021/acs.jmedchem.5b01374

Reference yield:

: 4530-20-5
BOC-glycine

: 701255-53-0
t-butyl (S)-(4-aminopentyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: (1,2-dimethoxyethane)dichloronickel(II); (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile; caesium carbonate; [2,2]bipyridinyl / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere; Irradiation

2: palladium 10% on activated carbon; hydrogen / methanol / Schlenk technique

With [2,2]bipyridinyl; (1,2-dimethoxyethane)dichloronickel(II); palladium 10% on activated carbon; (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile; hydrogen; caesium carbonate; In methanol; N,N-dimethyl-formamide;
DOI:10.1039/d1ob01624e