6-Maleimido-1-hexanol

Base Information

Chemical Name:6-Maleimido-1-hexanol
CAS No.:157503-18-9
Molecular Formula:C10H15NO3
Molecular Weight:197.234
Hs Code.:
DSSTox Substance ID:DTXSID60479910
Nikkaji Number:J2.140.735F
Wikidata:Q82314266
Mol file:157503-18-9.mol

Synonyms:6-Maleimido-1-hexanol;157503-18-9;1-(6-Hydroxyhexyl)-1H-pyrrole-2,5-dione;1-(6-HYDROXYHEXYL)PYRROLE-2,5-DIONE;1H-Pyrrole-2,5-dione, 1-(6-hydroxyhexyl)-;N-(6-hydroxyhexyl) maleimide;SCHEMBL307564;AMY487;DTXSID60479910;SVMIVBMALOISKL-UHFFFAOYSA-N;AKOS027439314;BS-53247;PD118214;FT-0670919;E77970;A907671;J-009418

Suppliers and Price of 6-Maleimido-1-hexanol

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
6-Maleimido-1-hexanol
100mg
$ 130.00

Total 10 raw suppliers

Chemical Property of 6-Maleimido-1-hexanol

Chemical Property:

Melting Point:48-51°C
Boiling Point:348.0±25.0 °C(Predicted)
PKA:15.17±0.10(Predicted)
PSA：64.71000
Density:1.179±0.06 g/cm3(Predicted)
LogP:1.39620
Storage Temp.:Room Temperature, Under Inert Atmosphere
Solubility.:DMSO (Slightly), Methanol (Slightly)
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:197.10519334
Heavy Atom Count:14
Complexity:230

Purity/Quality:

97% ^*data from raw suppliers

6-Maleimido-1-hexanol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=O)N(C1=O)CCCCCCO
Uses 6-Maleimido-1-hexanol is used in the preparation of water-soluble saccharide conjugates and saccharide mimetics by Diels-Alder reaction.

Technology Process of 6-Maleimido-1-hexanol

There total 4 articles about 6-Maleimido-1-hexanol 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: 76.0%

: 55750-48-6
N-methoxycarbonylmaleimide

: 4048-33-3
6-amino-1-hexanol

: 157503-18-9
1-(6-hydroxyhexyl)-1 H-pyrrole- 2,5-dione

Guidance literature:: With sodium hydrogencarbonate; In water; at 0 - 25 ℃;
DOI:10.1016/j.tet.2014.02.086

Reference yield: 54.0%

: 55750-53-3
2,5-Dihydro-2,5-dioxo-1H-pyrrole-1-hexanoic acid

: 157503-18-9
1-(6-hydroxyhexyl)-1 H-pyrrole- 2,5-dione

Guidance literature:: With borane-THF; In tetrahydrofuran; at 23 ℃; for 3h;

Reference yield: 25.0%

: 541-59-3,25721-74-8
maleiimide

: 4048-33-3
6-amino-1-hexanol

: 157503-18-9
1-(6-hydroxyhexyl)-1 H-pyrrole- 2,5-dione

Guidance literature:: maleiimide; With 4-methyl-morpholine; methyl chloroformate; In ethyl acetate; at 0 ℃; for 0.5h;

6-amino-1-hexanol; With sodium hydrogencarbonate; In water; ethyl acetate; for 0.5h;