sodium nitrite

Cc1c(I)ccc2c1C(=O)NS2(=O)=O
Reaction #906
iodine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cl.NNc1ccc(C(=O)O)c2c1CCCC2
Reaction #1178
hydrazine
Ausbeute 73.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(NN)ccc(C(=O)O)c1C.Cl
Reaction #1179
expected product
Ausbeute 93.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(C(=O)O)ccc1NN.Cl
Reaction #1180
4-Hydrazino-3-methoxybenzoic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cl.N#Cc1ccc(NN)cc1Cl
Reaction #1181
2-Chloro-4-hydrazinobenzonitrile hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cl.NNc1ccc(Cl)c(C(=O)O)c1
Reaction #1182
expected product
Ausbeute 123.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C(=O)O)cc1NN.Cl
Reaction #1183
3-Hydrazino-4-methylbenzoic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C(=O)O)ccc1I
Reaction #1232
3-methyl-4-iodobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C(=O)C(=NO)C(=O)c1c(C)cc(C)cc1C
Reaction #1249
semi-solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)[C@@H](Br)Cc1ccccc1
Reaction #1285
(S)-α-Bromobenzenepropanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC[C@H](Br)C(=O)O
Reaction #1291
crude title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(F)c(F)cc(F)c1C#N
Reaction #1368
2-methyl-3,4,6-trifluorobenzonitrile
Ausbeute 38.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)[C@@H](Br)Cc1ccccc1
Reaction #1419
(S)-α-Bromobenzenepropanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC[C@H](Br)C(=O)O
Reaction #1425
crude title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)C[C@H](Br)C(=O)O
Reaction #1427
crude title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1ccc(N=Nc2ccc([N+](=O)[O-])c(C(F)(F)F)c2)cc1
Reaction #3030
4-(3'-trifluoromethyl-4'-nitrophenyl)azobenzeneamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(Cl)cc([N+](=O)[O-])c1
Reaction #3232
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNc1nc(N=[N+]=[N-])ncc1C#N
Reaction #3257
title compound
Ausbeute 96.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1c2[nH]cnc2n(CC2CC2)c(=O)n1CC1CC1
Reaction #3739
1,3-Di-cyclopropylmethyl xanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCn1c(N)c(N=O)c(=O)n(CCC)c1=O
Reaction #3750
1,3-di-n-propyl-5-nitroso-6-aminouracil
Ausbeute 146.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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