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91679

Sigma-Aldrich

N-(6-Hydroxyhexyl)trifluoroacetamide

≥98.0% (GC)

Synonym(s):

6-(Trifluoroacetamido)-1-hexanol

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About This Item

Empirical Formula (Hill Notation):
C8H14F3NO2
CAS Number:
40248-34-8
Molecular Weight:
213.20
Beilstein:
1949232
MDL number:
MFCD00465535
UNSPSC Code:
12352200
PubChem Substance ID:
57653444
NACRES:
NA.22

Assay

≥98.0% (GC)

form

crystals

reaction suitability

reagent type: cross-linking reagent

mp

46-49 °C

SMILES string

OCCCCCCNC(=O)C(F)(F)F

InChI

1S/C8H14F3NO2/c9-8(10,11)7(14)12-5-3-1-2-4-6-13/h13H,1-6H2,(H,12,14)

InChI key

BGCYSPBEPMOQII-UHFFFAOYSA-N

Other Notes

Employed for preparing libraries of oligosaccharides with an amino tether

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
063322/1
63322/1

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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.

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