推薦產品
品質等級
化驗
≥99.0% (calc. based on dry substance, AT)
光學活性
[α]20/D +31.5±1.0°, c = 2% in H2O (dry matter)
反應適用性
reaction type: solution phase peptide synthesis
雜質
~1 mol water
應用
peptide synthesis
SMILES 字串
O.Cl.NCC(=O)N[C@@H](Cc1c[nH]cn1)C(O)=O
InChI
1S/C8H12N4O3.ClH.H2O/c9-2-7(13)12-6(8(14)15)1-5-3-10-4-11-5;;/h3-4,6H,1-2,9H2,(H,10,11)(H,12,13)(H,14,15);1H;1H2/t6-;;/m0../s1
InChI 密鑰
VGVLXWZHJBRECR-ILKKLZGPSA-N
尋找類似的產品? 前往 產品比較指南
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
Inorganic chemistry, 47(11), 4796-4807 (2008-05-08)
We have tested several computational protocols, at the nonrelativistic DFT level of theory, for the calculation of 1J(119Sn, 13C) and 2J(119Sn, 1H) spin-spin coupling constants in di- and trimethyltin(IV) derivatives with various ligands. Quite a good agreement with experimental data
Journal of inorganic biochemistry, 12(2), 143-156 (1980-04-01)
1H and 13C nmr studies on the Pd(II)Gly-His complex interaction with cytidine and GMP have shown that the nucleoside binds the palladium complex via N3 nitrogen and the nucleotide binds that complex via N7 nitrogen. The analysis of the Cyd
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 11(2), 153-167 (2005-12-13)
The pH dependence of redox properties, spectroscopic features and CO binding kinetics for the chelated protohemin-6(7)-L-histidine methyl ester (heme-H) and the chelated protohemin-6(7)-glycyl-L-histidine methyl ester (heme-GH) systems has been investigated between pH 2.0 and 12.0. The two heme systems appear
Inorganic chemistry, 43(21), 6674-6683 (2004-10-13)
Knowledge of the complexes formed by N-coordinating ligands and Cu(II) ions is of relevance in understanding the interactions of this ion with biomolecules. Within this framework, we investigated Cu(II) complexation with mono- and polydentate ligands, such as ammonia, ethylenediamine (en)
The journal of peptide research : official journal of the American Peptide Society, 56(4), 210-217 (2000-11-18)
The crystal structures of the complexes of oxalic acid with glycyl-L-histidine and L-histidyl-L-alanine were determined. The three crystallographically independent peptide molecules in the complexes have closed conformations. The terminal carboxyl group of the dipeptide and the oxalate ion in the
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