nitrite

O=NN(c1ccccc1)c1ccccc1
Reaction #7361
N-nitrosodiphenylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1c(O)cccc1C(=O)O
Reaction #8936
yellow solid
المردود 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN(C)c1ccc(N)cc1
Reaction #44401
p-aminodimethylaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1cc(I)ccc1S
Reaction #55727
5-iodothiosalicyclic acid
المردود 80.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=NCC(=O)Nc1ccccc1O
Reaction #57306
nitroso acetamidophenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)C(Br)Cc1ccc(OC)c(C(=O)NCc2ccc(C(F)(F)F)cc2)c1
Reaction #173528
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(Cl)cc(Br)cc1Cl
Reaction #173883
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Brc1cnc2nc(OCCN3CCOCC3)nc(N3CCOCC3)c2c1
Reaction #174011
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cc(F)ccc1Cl
Reaction #175117
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NNc1c(F)cccc1Br
Reaction #175406
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(CNC(=O)c1ccc(S(=O)(=O)Cl)c(F)c1)Oc1ccc(F)cc1
Reaction #175449
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(S(=O)(=O)N(Cc2ccccc2)N=O)cc1
Reaction #175621
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cc([N+](=O)[O-])cc(CC)c1-c1cc(S(N)(=O)=O)ccc1C
Reaction #175679
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(-c2ccccc2F)cc([N+](=O)[O-])c1NO
Reaction #175840
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1cnc2cccnc2c1
Reaction #175917
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCC1OC(=O)c2cc(C#N)ccc21
Reaction #176092
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCn1c(N)c(N=O)c(=O)[nH]c1=O
Reaction #176131
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)Cc1c[nH]c(N=Nc2ccc(C(=O)OC)cc2)n1
Reaction #176132
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(I)c(Cl)cc1C(=O)O
Reaction #176156
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1cnn(-c2ccc(Cl)cc2Cl)c1N=[N+]=[N-]
Reaction #176305
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي