91679
N-(6-Hydroxyhexyl)trifluoroacetamide
≥98.0% (GC)
Synonym(s):
6-(Trifluoroacetamido)-1-hexanol
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C8H14F3NO2
CAS Number:
Molecular Weight:
213.20
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1949232
Assay:
≥98.0% (GC)
Form:
crystals
InChI
1S/C8H14F3NO2/c9-8(10,11)7(14)12-5-3-1-2-4-6-13/h13H,1-6H2,(H,12,14)
SMILES string
OCCCCCCNC(=O)C(F)(F)F
InChI key
BGCYSPBEPMOQII-UHFFFAOYSA-N
assay
≥98.0% (GC)
form
crystals
reaction suitability
reagent type: cross-linking reagent
mp
46-49 °C
Other Notes
Employed for preparing libraries of oligosaccharides with an amino tether
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
M. Izumi et al.
Tetrahedron Letters, 39, 2079-2079 (1998)
Y Ichikawa et al.
Carbohydrate research, 198(2), 235-246 (1990-05-01)
A branched glycopeptide derivative incorporating two D-mannose 6-phosphate residues was prepared by coupling 6-aminohexyl 6-O-[bis(2,2,2-trichloroethoxy)phosphinyl]-alpha-D-mannopyranoside with N-acetyl-L-tyrosyl-L-aspart-oyldi-L-alanine followed by reductive deprotection of the phosphate group.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service