Urocanic acid

O=C(O)CCc1cnc[nH]1
Reaction #6861
3-(1H-Imidazol-5-yl)-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)CCc1c[nH]cn1
Reaction #429307
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=C(/C=C/c1c[nH]cn1)Oc1ccc([N+](=O)[O-])cc1
Reaction #813420
p-Nitrophenyl trans-3-(1H-imidazol-4-yl)-2-propenoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
O=C(/C=C/c1c[nH]cn1)Oc1ccc([N+](=O)[O-])cc1
Reaction #831228
p-Nitrophenyl trans-3-(1H-imidazol-4-yl)-2-propenoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
O=C(O)CCc1c[nH]cn1
Reaction #986794
solid
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
O=C(O)CCc1c[nH]cn1
Reaction #986939
solid
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
O=C(O)CCc1cnc[nH]1
Reaction #988297
3-(1H-Imidazol-5-yl)-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
O=C(O)CCc1c[nH]cn1
Reaction #1095849
3-(1H-Imidazol-4-yl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
CN(CCNC(=O)C=Cc1c[nH]cn1)CCNc1ccnc2cc(Cl)ccc12
Reaction #1095850
N-(2-{[2-(7-Chloro-quinolin-4-ylamino)ethyl]methylamino}ethyl)-3-(1H-imidazol-4-yl)acrylamide
Выход 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
N.N[C@@H](Cc1c[nH]cn1)C(=O)O
Reaction #1114533
Histidine Ammonia
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
O=C(O)CCc1c[nH]cn1
Reaction #1154838
3-(4-imidazolyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_06
COC(=O)C=Cc1c[nH]cn1
Reaction #1195685
crude product 2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_05
O=C(/C=C/c1c[nH]cn1)Oc1ccc([N+](=O)[O-])cc1
Reaction #1474334
p-Nitrophenyl trans-3-(1H-imidazol-4-yl)-2-propenoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_07
N[C@@H](Cc1c[nH]cn1)C(=O)O
Reaction #1477379
L-histidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_02
O=C(O)CCc1c[nH]cn1
Reaction #1711438
solid
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
O=C(/C=C/c1c[nH]cn1)N1CCN(C2c3ccc(Cl)cc3CCc3cccnc32)CC1
Reaction #1721763
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_01
COC(=O)C=Cc1c[nH]cn1
Reaction #1827242
crude product 2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_10
N.N[C@@H](Cc1c[nH]cn1)C(=O)O
Reaction #1835894
Histidine Ammonia
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10