N-(2,4-dinitrophenyl)-L-proline

chemical compound

C₁₁H₁₁N₃O₆

N-(2,4-dinitrophenyl)-L-proline is …
instance of (P31):
type of chemical entityQ113145171

sublass of (P279):
N-(2,4-dinitrophenyl)prolineQ27123955

External links are
P233canonical SMILESC1CC(N(C1)C2=C(C=C(C=C2)[N+](=O)[O-])[N+](=O)[O-])C(=O)O
P231CAS Registry Number1655-55-6
P683ChEBI ID53086
P661ChemSpider ID87407
P3117DSSTox substance IDDTXSID501303696
P232EC number216-743-0
P2566ECHA Substance Infocard ID100.015.222
P234InChIInChI=1S/C11H11N3O6/c15-11(16)9-2-1-5-12(9)8-4-3-7(13(17)18)6-10(8)14(19)20/h3-4,6,9H,1-2,5H2,(H,15,16)/t9-/m0/s1
P235InChIKeyMVZXUWLTGGBNHL-VIFPVBQESA-N
P2017isomeric SMILESC1C[C@H](N(C1)C2=C(C=C(C=C2)[N+](=O)[O-])[N+](=O)[O-])C(=O)O
P2840NSC number89618
P662PubChem CID96807
P1579Reaxys registry number93597
5608202
P11089UniChem compound ID1100109

P2067mass281.064785
P3364stereoisomer of1-(2,4-Dinitrophenyl)-D-prolineQ82241313

Reverse relations

main subject (P921)
Q44085533Reversal of elution order of N-(2,4-dinitrophenyl)-proline and N-(2,4-dinitrophenyl)-serine in HPLC by BSA chiral stationary phase
Q43205446The specificity of cross‐reactivity: Promiscuous antibody binding involves specific hydrogen bonds rather than nonspecific hydrophobic stickiness

Q822413131-(2,4-Dinitrophenyl)-D-prolinestereoisomer ofP3364

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