chloroethyl chloroformate

CC(Cl)OC(=O)c1ncc[nH]1
Reaction #4527
α-chloroethoxycarbonylimidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC(=O)[C@H]1CC[C@H](NC(=O)OCCCl)CC1
Reaction #44973
methyl trans-4-{[(2-chloroethoxy)carbonyl]amino}cyclohexanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cl
Reaction #58566
HCl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1cccc(C)c1NNC(=O)OCCCl
Reaction #96186
2-Chloroethyl 2-(2,6-dimethylphenyl)-hydrazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Brc1cc(N2CCNCC2)c2ncccc2c1
Reaction #177840
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(N2CCOC2=O)ccc1-c1nc2c(c(C3CCCCC3)nn2C)c(=O)[nH]1
Reaction #189046
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc(NC(=O)OCCCl)cc1[N+](=O)[O-]
Reaction #202247
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C(=O)O)c1ccc(NC(=O)OCCCl)cc1
Reaction #208093
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1ccc2c(c1)C1(CCNCC1)OC2
Reaction #224557
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(N)c([N+](=O)[O-])cc1NC(=O)OCCCl
Reaction #232452
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(-c2csc(N3CCOC3=O)n2)cc1
Reaction #241943
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(OC)c([N+](=O)[O-])c(OC)c1NC(=O)OCCCl
Reaction #245387
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NCC1CCC(Nc2nc3c(s2)CCCc2ccc(F)cc2-3)CC1)OCCCl
Reaction #296490
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cl.c1ccc(-c2noc(C3CNCCO3)n2)cc1
Reaction #305506
2-(3-Phenyl-[1,2,4]oxadiazol-5-yl)-morpholine Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cl.c1ccc(-c2nc(C3CNCCO3)no2)cc1
Reaction #305510
2-(5-Phenyl-[1,2,4]oxadiazol-3-yl)-morpholine Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CS(=O)(=O)OC1CNC1.Cl
Reaction #309503
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CS(=O)(=O)OC1CNC1.Cl
Reaction #312986
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
O=C1OCCN1c1ccccc1[C@@H]1CN(C2CC2)Cc2c(Cl)cc(Cl)cc21
Reaction #339057
desired product
수율 132.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CN1Cc2c(Cl)cc(Cl)cc2[C@H](c2ccccc2N2CCOC2=O)C1
Reaction #339058
desired product
수율 108.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
O=C(Nc1ccc(CC(F)(F)F)c([N+](=O)[O-])c1)OCCCl
Reaction #344426
2-chloroethyl-N-[4-(2,2,2-trifluoroethyl)-3-nitrophenyl]-carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
1 페이지다음 페이지