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About This Item
Empirical Formula (Hill Notation):
C10H15F6N6OP
CAS Number:
Molecular Weight:
380.23
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.22
Product Name
HATU, 97%
Quality Level
assay
97%
form
solid
reaction suitability
reaction type: Coupling Reactions
mp
183-185 °C (lit.)
application(s)
peptide synthesis
functional group
amine
storage temp.
2-8°C
SMILES string
F[P-](F)(F)(F)(F)F.CN(C)[C+](N(C)C)n1n[n+]([O-])c2ncccc12
InChI
1S/C10H15N6O.F6P/c1-13(2)10(14(3)4)15-8-6-5-7-11-9(8)16(17)12-15;1-7(2,3,4,5)6/h5-7H,1-4H3;/q+1;-1
InChI key
FKBFHOSFPRWJNV-UHFFFAOYSA-N
Application
Peptide coupling reagent.
Preparation of N-arylsulfonamide-linked peptides by solid-phase synthesis.
Reagent for:
Synthesis of Aurora A kinase inhibitors
HPLC assay to determine D- and L- acid enantiomers in human plasma
Amide bond formation reactions
Catalyst for:
Selective acylation
Selecocyclization-oxidation deselenation sequence
Synthesis of Aurora A kinase inhibitors
HPLC assay to determine D- and L- acid enantiomers in human plasma
Amide bond formation reactions
Catalyst for:
Selective acylation
Selecocyclization-oxidation deselenation sequence
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signalword
Danger
hcodes
Hazard Classifications
Resp. Sens. 1 - Skin Sens. 1A
supp_hazards
Storage Class
4.1A - Other explosive hazardous materials
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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Find documentation for the products that you have recently purchased in the Document Library.
Pept., Proceedings of the European Peptide Symposium., ed. U. Ragnarrson, 27, 272-273 (2002)
J. Prakt. Chem./Chem.-Ztg., 340, 581-583 (1998)
Lett. Pept. Sci., 9, 119-123 (2003)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 445460-25G | 04061832283951 |
| 445460-5G | 04061832283968 |
| 445460-100G | 04061832283845 |
| 445460-1G | 04061832283890 |
