hydroxylamine hydrochloride

CC(=O)O[C@H]1CC[C@H]2[C@@H]3CC[C@H]4CC(=NO)C(=NO)C[C@]4(C)[C@H]3CC[C@]12C
Reaction #928
17β-Acetoxy-2,3-dihydroxyimino-5α-androstane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)C(=NO)C(=O)O
Reaction #1394
trimethylpyruvic acid oxime
Yield 81.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCn1c(C2=CC=CC(=NO)C2)nc(CC)c(CC)c1=O
Reaction #1555
5,6-diethyl-2-(3-hydroxyiminophenyl)-3-propargyl-4(3H)-pyrimidinone
Yield 77.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
ON=C1CCCc2ccccc21
Reaction #1828
product
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)S(=O)(=O)C1=CCC(=NO)C=C1
Reaction #2568
title compound
Yield 102.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCN1CC[C@]2(c3cccc(OC)c3)CC(=NO)CC[C@H]2C1
Reaction #2955
title compound
Yield 96.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(NC(=O)C=NO)c1
Reaction #3203
title compound
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccccc1)c1ccccc1SSc1ccccc1C(=NO)c1ccccc1
Reaction #3843
title compound
Yield 35.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1c2ccccc2C(=O)N1C1N=CC(C(Cl)Cl)=NC1=NO
Reaction #4538
colorless crystals
Yield 67.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCC(=NO)c1noc(COc2ccc(Cl)cc2Cl)n1
Reaction #4994
desired product
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)c1c(C=NO)cccc1Oc1nc(OC)cc(OC)n1
Reaction #5001
aimed compound
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(c1ccccc1)c1cc(C)c2c(c1O)C(=NO)CC2
Reaction #5097
2,3-dihydro-7-hydroxy-4-methyl-6-(1-phenyl-2-propenyl)-1H-inden-1-one oxime
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CNC(=O)C[n+]1ccccc1-c1cc(C)c2c(c1O)C(=NO)CC2.[Cl-]
Reaction #5099
(2,3-dihydro-7-hydroxy-1-hydroxyimino-4-methyl-1H-indene-6yl)-methylaminocarbonylmethylpyridinium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
—
Reaction #5327
product
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCc1nc2cccc(C(=S)OC)c2n1Cc1ccc(-c2ccccc2C(=N)NO)cc1
Reaction #5330
title compound
Yield 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
ON=CC12CCCN(CCC1)C2
Reaction #5460
colorless crystals
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)CCCCCO/N=C1/c2ccccc2OC(c2ccccc2)C1n1ccnc1
Reaction #6077
(+-)-(Z)-Ethyl-6-[[2-phenyl-3-(1H-imidazol-1-yl)-2,3-dihydro-4H-benzopyranylidene]aminoxy]hexanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1c2cccc3cccc(c23)C(=O)N1O
Reaction #6709
N-hydroxynaphthalimide
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)C(=O)NC1CCN(c2ccc3cc(C(=N)NO)ccc3n2)C1
Reaction #6910
N-(1-{6-[(Hydroxyamino)(imino)methyl]quinolin-2-yl}pyrrolidin-3-yl)-2,2-dimethylpropanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=c1[nH]cc(CO)c(=O)[nH]1
Reaction #7320
5-(hydroxymethyl)-1,3-dihydropyrimidine-2,4-dione
Yield 14.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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