10-(t-Boc-amino)-1-decylbromide

Base Information

Chemical Name:10-(t-Boc-amino)-1-decylbromide
CAS No.:887353-29-9
Molecular Formula:C₁₅H₃₀BrNO₂
Molecular Weight:336.313
Hs Code.:
DSSTox Substance ID:DTXSID10405163
Wikidata:Q82209583
Mol file:887353-29-9.mol

Synonyms:10-(t-Boc-amino)-1-decylbromide;887353-29-9;tert-Butyl (10-bromodecyl)carbamate;Tert-butyl N-(10-bromodecyl)carbamate;10-(Boc-amino)-1-decyl bromide;SCHEMBL19460948;10-(Boc-amino)-1-decylbromide;DTXSID10405163;AKOS025295878;AB92444;AT10273;MS-21850;CS-0119811;FT-0663435;A905565;A1-23333

Suppliers and Price of 10-(t-Boc-amino)-1-decylbromide

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
10-(t-Boc-amino)-1-decylbromide
100mg
$ 425.00

Medical Isotopes, Inc.
10-(t-Boc-amino)-1-decylbromide
25 mg
$ 830.00

Biosynth Carbosynth
10-(t-Boc-amino)-1-decylbromide
1 g
$ 1000.00

Biosynth Carbosynth
10-(t-Boc-amino)-1-decylbromide
50 mg
$ 400.00

Biosynth Carbosynth
10-(t-Boc-amino)-1-decylbromide
500 mg
$ 700.00

Biosynth Carbosynth
10-(t-Boc-amino)-1-decylbromide
250 mg
$ 600.00

Biosynth Carbosynth
10-(t-Boc-amino)-1-decylbromide
100 mg
$ 500.00

American Custom Chemicals Corporation
10-(T-BOC-AMINO)-1-DECYLBROMIDE 95.00%
25MG
$ 704.55

American Custom Chemicals Corporation
10-(T-BOC-AMINO)-1-DECYLBROMIDE 95.00%
250MG
$ 1593.90

AK Scientific
10-(t-Boc-amino)-1-decylbromide
1g
$ 1400.00

Total 8 raw suppliers

Chemical Property of 10-(t-Boc-amino)-1-decylbromide

Chemical Property:

Vapor Pressure:1.69E-06mmHg at 25°C
Melting Point:35-37°C
Boiling Point:396.6°C at 760 mmHg
Flash Point:193.6°C
PSA：41.82000
Density:1.114g/cm³
LogP:5.23120
Storage Temp.:-20°C Freezer
Solubility.:Chloroform (Slightly), Methanol (Slightly)
XLogP3:5.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:12
Exact Mass:335.14599
Heavy Atom Count:19
Complexity:227

Purity/Quality:

97% ^*data from raw suppliers

10-(t-Boc-amino)-1-decylbromide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NCCCCCCCCCCBr

Technology Process of 10-(t-Boc-amino)-1-decylbromide

There total 5 articles about 10-(t-Boc-amino)-1-decylbromide 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: 92.0%

: 173606-54-7
(10-hydroxydecyl)carbamic acid tert-butyl ester

: 887353-29-9
1-[10-(2,3,4,6-O-tetrabenzoyl-β,D-glucopyranos-1-yl)-1-oxodecyl]-4,11-bis-(t-butoxycarbonylmethyl)-8-(10-(t-butoxycarbonylamino)decyl)-1,4,8,11-tetraazacyclotetradecane

Guidance literature:: With carbon tetrabromide; triphenylphosphine; In dichloromethane;
DOI:10.1016/j.nucmedbio.2021.01.001

Reference yield:

: 53463-68-6
1-bromo-10-decanol

: 887353-29-9
1-[10-(2,3,4,6-O-tetrabenzoyl-β,D-glucopyranos-1-yl)-1-oxodecyl]-4,11-bis-(t-butoxycarbonylmethyl)-8-(10-(t-butoxycarbonylamino)decyl)-1,4,8,11-tetraazacyclotetradecane

Guidance literature:: Multi-step reaction with 4 steps

1: N,N-dimethyl-formamide / 20 h / 100 °C

2: hydrazine hydrate / ethanol / Reflux

3: dichloromethane; methanol / 2.5 h / 0 - 5 °C

4: triphenylphosphine; carbon tetrabromide / dichloromethane / 2.5 h / Inert atmosphere

With carbon tetrabromide; hydrazine hydrate; triphenylphosphine; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 161270-70-8
2-(10-hydroxydecyl)-1H-isoindole-1,3(2H)-dione

: 887353-29-9
1-[10-(2,3,4,6-O-tetrabenzoyl-β,D-glucopyranos-1-yl)-1-oxodecyl]-4,11-bis-(t-butoxycarbonylmethyl)-8-(10-(t-butoxycarbonylamino)decyl)-1,4,8,11-tetraazacyclotetradecane

Guidance literature:: Multi-step reaction with 3 steps

1: hydrazine hydrate / ethanol / Reflux

2: dichloromethane; methanol / 2.5 h / 0 - 5 °C

3: triphenylphosphine; carbon tetrabromide / dichloromethane / 2.5 h / Inert atmosphere

With carbon tetrabromide; hydrazine hydrate; triphenylphosphine; In methanol; ethanol; dichloromethane;