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Informacje o tej pozycji
Wzór liniowy:
H2NCH2CO2C(CH3)3 · HCl
Numer CAS:
Masa cząsteczkowa:
167.63
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352200
MDL number:
Beilstein/REAXYS Number:
3989048
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Pomoc techniczna
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Pozwól nam pomócgrade
puriss.
Quality Level
assay
≥99.0% (AT)
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
141-143 °C (lit.)
solubility
H2O: 0.1 g/mL, clear, colorless
application(s)
peptide synthesis
SMILES string
Cl.CC(C)(C)OC(=O)CN
InChI
1S/C6H13NO2.ClH/c1-6(2,3)9-5(8)4-7;/h4,7H2,1-3H3;1H
InChI key
OSWULUXZFOQIRU-UHFFFAOYSA-N
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Klasa składowania
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
M Nakoji et al.
Organic letters, 3(21), 3329-3331 (2001-10-12)
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Baptiste Thierry et al.
Molecular diversity, 9(4), 277-290 (2005-11-29)
Cross-linked polystyrene-bound and poly(ethylene glycol)-bound phase-transfer catalysts as well as homopolymers of cinchona alkaloid derivatives have been synthesised. Both soluble and insoluble polymers have been investigated. The enantioselective alkylation of N-diphenyl methylene glycine t-butyl ester has been successfully carried out
S Sarhan et al.
Arzneimittel-Forschung, 34(6), 687-690 (1984-01-01)
The synergistic amplification of the anticonvulsant effects of direct and indirect GABA agonists by glycine has previously been demonstrated. We show in the present report that the anticonvulsant effect of vinyl GABA, a GABA-T (4-aminobutyrate: 2-oxoglutarate aminotransferase) inhibitor with antiepileptic
Ming-Qing Hua et al.
Chemical communications (Cambridge, England), 47(5), 1631-1633 (2010-12-01)
An efficient, catalytic, diastereo- and enantioselective conjugate addition of N-(diphenylmethylene)glycine tert-butyl ester to β-aryl substituted enones was realized in the presence of 1 mol% of newly desired dinuclear N-spiro-ammonium salts, affording functionalized α-amino acid derivatives in 57-98% yields with high
V De Filippis et al.
Biochemistry, 37(39), 13507-13515 (1998-09-30)
Hirudin is the most potent and specific inhibitor of thrombin, a key enzyme in the coagulation process existing in equilibrium between its procoagulant (fast) and anticoagulant (slow) form. In a previous study, we described the solid-phase synthesis of a Trp3
Numer pozycji handlu globalnego
| SKU | NUMER GTIN |
|---|---|
| 02568-5ML | 04061837082504 |
| 42604-1G-F | 04061826663325 |
| 42604-5G-F | 04061833348420 |
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