3,5-Dimethyl-1H-pyrazole-1-carboximidamide nitrate
3,5-Dimethyl-1H-pyrazole-1-carboximidamide nitrate structure
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Common Name | 3,5-Dimethyl-1H-pyrazole-1-carboximidamide nitrate | ||
|---|---|---|---|---|
| CAS Number | 38184-47-3 | Molecular Weight | 201.183 | |
| Density | N/A | Boiling Point | 265.8ºC at 760 mmHg | |
| Molecular Formula | C6H11N5O3 | Melting Point | 167-168ºC (dec.)(lit.) | |
| MSDS | Chinese USA | Flash Point | 114.6ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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The solid-phase synthesis of side-chain-phosphorylated peptide-4-nitroanilides.
J. Pept. Res. 50(2) , 143-52, (1997) Peptide-4-nitroanilides can be quickly synthesised using an Fmoc-based approach on 2-chlorotritylchloride resin. Preformed building blocks Fmoc-Xaa-NH-Np (Xaa = Cit, Cys, Gln, His, Lys, Orn, Ser, Thr, Tyr, Trp) can be attached via side chain to the 2-chlorotr... |
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Assessment of protein function following cross-linking by alpha-dicarbonyls.
Ann. N. Y. Acad. Sci. 1043 , 195-200, (2005) Protein cross-linking via the Maillard reaction with alpha-dicarbonyl compounds has been the subject of intense scrutiny in the literature. We report here a study of the impact of this cross-linking on enzyme function. Protein function following glycation was... |
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FT-IR and theoretical study of 3,5-dimethyl-1H-pyrazole-1-carboxamidine (L) and the complexes CoL2(H2O)2(NO3)2, NiL2(H2O)2(NO3)2.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 71(4) , 1466-73, (2008) In the paper a joint experimental and theoretical study of 3,5-dimethyl-1H-pyrazole-1-carboxamidine (L) as well as its complexes CoL2(H2O)2(NO3)2 and NiL2(H2O)2(NO3)2 is reported. On the basis of FT-IR experiments and a DFT-derived scaled quantum mechanical f... |
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Guanidination and nitroguanidination of staphylococcal enterotoxin B.
Biochim. Biophys. Acta 251(3) , 345-56, (1971) Guanidination of the free amino groups of staphylococcal enterotoxin B with 3,5-dimethyl-1-guanylpyrazole converted 31-32 of 33 epsilon-amino groups and 30% of the N-terminal residue. This product, although markedly reduced in solubility, suffered no gross ch... |
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J. Carbohydr. Chem. 12 , 1173, (1993)
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