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About This Item
Empirical Formula (Hill Notation):
C6H8ClN2O5P
CAS Number:
Molecular Weight:
254.56
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3654596
Assay:
≥97.0% (AT)
Form:
solid
Quality Level
assay
≥97.0% (AT)
form
solid
mp
191 °C (dec.) (lit.)
SMILES string
ClP(=O)(N1CCOC1=O)N2CCOC2=O
InChI
1S/C6H8ClN2O5P/c7-15(12,8-1-3-13-5(8)10)9-2-4-14-6(9)11/h1-4H2
InChI key
KLDLRDSRCMJKGM-UHFFFAOYSA-N
Application
Bis(2-oxo-3-oxazolidinyl)phosphinic chloride was used in the preparation of hexadepsipeptide.
Other Notes
Reagent for activating the carboxylic group, synthesis of amides ; Esters ; Peptides
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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R.D. Tung et al.
Journal of the American Chemical Society, 107, 4342-4342 (1985)
Yanjie Xu et al.
Molecules (Basel, Switzerland), 10(1), 259-264 (2007-11-17)
Hexadepsipeptide 2, the precursor of Hirsutellide A (1), was synthesized in an overall yield of 45% from N-Boc-Me-Gly via three coupling reactions using dicyclohexylcarbodiimide (DCC), O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyl- uronium hexafluorophosphate (HATU) and bis(2-oxo-3-oxazolidinyl)phosphinic chloride (BOP-Cl), respectively.
E.J. Corey et al.
Journal of the American Chemical Society, 104, 6818-6818 (1982)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 15140-5G | 04061838739186 |
| 15140-25G | 04061833416570 |
