1-Boc-1,8-diaminooctane

Base Information

Chemical Name:1-Boc-1,8-diaminooctane
CAS No.:88829-82-7
Molecular Formula:C13H28N2O2
Molecular Weight:244.378
Hs Code.:2924199090
Mol file:88829-82-7.mol

Synonyms:Carbamicacid, (8-aminooctyl)-, 1,1-dimethylethyl ester (9CI);Boc-1,8-diaminooctane;tert-Butyl (8-aminooctyl)carbamate;

Suppliers and Price of 1-Boc-1,8-diaminooctane

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

Usbiological
1-Boc-1,8-diaminooctane
100mg
$ 305.00

TRC
1-Boc-1,8-diaminooctane
250mg
$ 45.00

TRC
1-Boc-1,8-diaminooctane
500mg
$ 70.00

SynQuest Laboratories
Octane-1,8-diamine, N-Boc protected 97%
5 g
$ 676.00

SynQuest Laboratories
Octane-1,8-diamine, N-Boc protected 97%
25 g
$ 2024.00

SynQuest Laboratories
Octane-1,8-diamine, N-Boc protected 97%
1 g
$ 212.00

Crysdot
tert-Butyl(8-aminooctyl)carbamate 95+%
5g
$ 313.00

Crysdot
tert-Butyl(8-aminooctyl)carbamate 95+%
1g
$ 95.00

Biosynth Carbosynth
1-Boc-1,8-diaminooctane
500 mg
$ 160.00

Biosynth Carbosynth
1-Boc-1,8-diaminooctane
100 mg
$ 60.00

Total 22 raw suppliers

Chemical Property of 1-Boc-1,8-diaminooctane

Chemical Property:

Vapor Pressure:2.96E-05mmHg at 25°C
Refractive Index:1.461
Boiling Point:356.3 °C at 760 mmHg
Flash Point:169.3 °C
PSA：64.35000
Density:0.942 g/cm³
LogP:3.90160
Storage Temp.:under inert gas (nitrogen or Argon) at 2–8 °C
Solubility.:Chloroform, Methanol

Purity/Quality:

99%, ^*data from raw suppliers

1-Boc-1,8-diaminooctane ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi

MSDS Files:: SDS file from LookChem

Useful:

Description tert-butyl (8-aminooctyl)carbamate can be used as a PROTAC linker in the synthesis of PROTACs. tert-butyl (8-aminooctyl)carbamate is an alkane chain with terminal amine and Boc-protected amino groups. Amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine.

Technology Process of 1-Boc-1,8-diaminooctane

There total 15 articles about 1-Boc-1,8-diaminooctane 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: 100.0%