365963
N,N-二乙基亚磷酰胺二叔丁酯
technical grade, 93%
别名:
Bis(1,1-dimethylethyl) N,N-diethylphosphoramidite, Di-tert-butyl diethylphosphoramidite
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关于此项目
线性分子式:
(C2H5)2NP[OC(CH3)3]2
化学文摘社编号:
分子量:
249.33
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4175262
Assay:
93%
Form:
liquid
产品名称
N,N-二乙基亚磷酰胺二叔丁酯, technical grade, 93%
InChI
1S/C12H28NO2P/c1-9-13(10-2)16(14-11(3,4)5)15-12(6,7)8/h9-10H2,1-8H3
SMILES string
CCN(CC)P(OC(C)(C)C)OC(C)(C)C
InChI key
KUKSUQKELVOKBH-UHFFFAOYSA-N
grade
technical grade
assay
93%
form
liquid
refractive index
n20/D 1.434 (lit.)
bp
39-41 °C/0.3 mmHg (lit.)
density
0.896 g/mL at 25 °C (lit.)
functional group
amine
storage temp.
2-8°C
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
172.4 °F - closed cup
flash_point_c
78 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
J W Perich et al.
Bioorganic & medicinal chemistry, 4(2), 143-150 (1996-02-01)
The seven phosphopeptide derivatives based on the native -NEYTA- sequence of the pp60src protein kinase family, Asn-Glu-Tyr(P)-Ser-Ala, Ala-Glu-Tyr(P)-Ser-Ala, Ala-Ser-Tyr(P)-Ser-Ala, Ala-Ser(P)-Tyr-Ser-Ala, Ala-Thr-Tyr(P)-Ser-Ala, Ala-Thr(P)-Tyr-Ser-Ala and Ala-Ser(P)-Tyr(P)-Ser-Ala, were prepared in good yield using the "global' "phosphite-triester' phosphorylation method. The peptide resins were assembled
Calcium phosphate nanoparticles: colloidally stabilized and made fluorescent by a phosphate-functionalized porphyrin.
Ganesan K, et al.
Journal of Materials Chemistry, 18(31), 3655-3661 (2008)
H Mostafavi et al.
Biomedical peptides, proteins & nucleic acids : structure, synthesis & biological activity, 1(5), 255-260 (1995-01-01)
Based on the global phosphorylation approach, a selective synthesis of (Ser10-phosphatidyl)-urodilatin (phosphourodilatin), which contains 32 amino acid residues and a disulfide loop is described. The peptide was assembled stepwise on a polyethyleneglycol-polystyrene support using Fmoc-chemistry. The phosphorylation was performed on-resin
D Dunn et al.
The Journal of biological chemistry, 271(1), 168-173 (1996-01-05)
Yersinia protein-tyrosine phosphatase substrates have been synthesized employing an expedient methodology that incorporates phosphorylated non-amino acid residues into an active site-directed peptide. While the peptidic portion of these compounds serves an enzyme targeting role, the nonpeptidic component provides a critical
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