chloroacetyl chloride

O=C(CCl)Nc1ccccn1
Reaction #993
brown solid
收率 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CCl)NNC(=O)c1ccc(Cl)cc1
Reaction #1609
N'-chloroacetyl-4-chlorobenzoic hydrazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CCl)NNC(=O)c1ccc(Cl)cc1
Reaction #1677
N'-chloroacetyl-4-chlorobenzoic hydrazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CCl)NNC(=O)c1ccc(Cl)cc1
Reaction #2182
N'-chloroacetyl-4-chlorobenzoic hydrazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CCl)NNC(=O)c1ccc(Cl)cc1
Reaction #2223
N'-chloroacetyl-4-chlorobenzoic hydrazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CCl)NNC(=O)c1ccc(Cl)cc1
Reaction #2281
N'-chloroacetyl-4-chlorobenzoic hydrazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NC(=O)N1CCOCC1.O=C(O)CCl
Reaction #2799
chloroacetic acid morpholine carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CCl)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
Reaction #3692
beige solid
收率 100.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CCl)Nc1ccc(OCc2ccccc2)c(OCc2ccccc2)c1
Reaction #4208
2-Chloro-N-[3,4-bis(phenylmethoxy)phenyl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C(CCl)Nc1ccc(F)c(Cl)c1
Reaction #4565
N-(2-chloroacetyl)-3-chloro-4-fluoroaniline
收率 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cl.O=C(CCl)NC1CN2CCC1CC2
Reaction #5597
solid
收率 144.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1COc2ccc3ccccc3c2N1
Reaction #5930
1H-naphtho[2,1-b][1,4]oxazin-2(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(CCl)N1C[C@@H](c2ccc(Cl)cc2)Sc2ccccc21
Reaction #5936
(R)-4-chloroacetyl-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine
收率 108.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
—
Reaction #7014
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(CCl)NNc1c(Cl)cc(C(F)(F)F)cc1Cl
Reaction #8517
title compound
收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(CCl)N1CCCN(c2ccc([N+](=O)[O-])cc2)CC1
Reaction #8647
yellow crystals
收率 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(CCl)NCc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10054
product
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2Cc3c(NC(=O)CCl)cccc3C2=O)C(=O)N1
Reaction #10084
product
收率 92.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)CCl
Reaction #11721
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)CCl
Reaction #11727
title compound
收率 84.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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