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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
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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.
M. Izumi et al.
Tetrahedron Letters, 39, 2079-2079 (1998)
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