BOC-1,5-DIAMINOPENTANE HYDROCHLORIDE

Base Information

Chemical Name:BOC-1,5-DIAMINOPENTANE HYDROCHLORIDE
CAS No.:77835-31-5
Molecular Formula:C10H23ClN2O2
Molecular Weight:0
Hs Code.:2924199090
Mol file:77835-31-5.mol

Synonyms:N-BOC-1,5-DIAMINOPENTANE HYDROCHLORIDE;Boc-1,5-diaminopentane·HCl≥ 98% (Titration)

Suppliers and Price of BOC-1,5-DIAMINOPENTANE HYDROCHLORIDE

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
Boc-dapehydrochloride
100mg
$ 85.00

Iris Biotech GmbH
Boc-DAPe*HCl
5 g
$ 303.75

Iris Biotech GmbH
Boc-DAPe*HCl
25 g
$ 1215.00

Crysdot
tert-Butyl(5-aminopentyl)carbamatehydrochloride 95+%
5g
$ 602.00

CHESS?
N-Boc-1,5-diaminopentanexHCl 98
5 g
$ 18000.00

CHESS?
N-Boc-1,5-diaminopentanexHCl 98
1 g
$ 6000.00

Biosynth Carbosynth
Boc-1,5-diaminopentane·HCl
5 g
$ 368.00

Biosynth Carbosynth
Boc-1,5-diaminopentane·HCl
2 g
$ 230.00

Biosynth Carbosynth
Boc-1,5-diaminopentane·HCl
1 g
$ 143.80

Biosynth Carbosynth
Boc-1,5-diaminopentane·HCl
500 mg
$ 60.00

Total 8 raw suppliers

Chemical Property of BOC-1,5-DIAMINOPENTANE HYDROCHLORIDE

Chemical Property:

PSA：78.34000
LogP:2.98700

Purity/Quality:

99% ^*data from raw suppliers

Boc-dapehydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Building block for preparing polyamines and polyamides.

Technology Process of BOC-1,5-DIAMINOPENTANE HYDROCHLORIDE

There total 6 articles about BOC-1,5-DIAMINOPENTANE HYDROCHLORIDE 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: 95.0%

: 129392-86-5
(5-azido-pentyl)carbamic acid tert-butyl ester

: 77835-31-5
N-(tert-butoxycarbonyl)-1,5-diaminopentane hydrochloride

Guidance literature:: With chloroform; hydrogen; palladium on activated charcoal; In methanol; for 1h; under 1551.4 Torr;
DOI:10.1055/s-1990-26879

Reference yield: 62.7%

: 462-94-2
1,5-diaminopentane

: 24424-99-5
di-tert-butyl dicarbonate

: 77835-31-5
N-(tert-butoxycarbonyl)-1,5-diaminopentane hydrochloride

Guidance literature:: With triethylamine; In tetrahydrofuran; methanol; for 1h;
DOI:10.1016/S0040-4020(01)86395-X

Reference yield:

: 2508-29-4
5-hydroxypentylamine

: 77835-31-5
N-(tert-butoxycarbonyl)-1,5-diaminopentane hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / CH₂Cl₂ / 12 h

2: triethylamine / toluene / 0.08 h / 0 °C

3: NaN₃ / tetrabutylammonium bromide / toluene; H₂O / 3 h / 60 °C

4: 95 percent / H₂, CHCl₃ / Pd-C / methanol / 1 h / 1551.4 Torr

With sodium azide; chloroform; hydrogen; triethylamine; palladium on activated charcoal; tetrabutylammomium bromide; In methanol; dichloromethane; water; toluene;
DOI:10.1055/s-1990-26879