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CAS:3173-72-6
Molecular Formula:C12H6N2O2
Alias
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Naphthyl 1,5-Diisocyanate; 1,5-Diisocyanatonaphthalene; NDI; 1,5-Naphthalene Diis; Desmodur15; 1,5-Naphthyldiisocyanate; Naphthalene Diisocyanate; 1,5-Ndi; 1,5-Naphalene Diisocyanate; Naphthalene 1,5-Diisocyanate; 1,5-Diisocyanato-Naphthalene; 1,5-Naphthalene; 1,5-Naphthalenediisocyanate; 5-Naphthylene Diisocyanate; Naphthylenediisocyanate; 1,5-Naphthylene Diisocyanate
Brief Introduction
Used as pesticide and pharmaceutical intermediate.
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CAS:320-67-2
Molecular Formula:C8H12N4O5
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Vidaza; Ladakamycin; 5-Azacitidine; Azacitidine; 5-Ac; 5-Azac; Azgr; 5 Azc; [14C]-Azacitidine; 5-Azcr; 5-Ac-15N4; 5'-Azacytidine; Mylosar; 1,3,5-Triazine-2(1H)-One, 4-Amino-1-α-D-Ribofuranosyl-
Brief Introduction
Antimetabolic drugs. The main indication is acute myeloid leukemia which is ineffective to conventional treatment. It is also used for breast cancer, melanoma, intestinal cancer and so on. The main manifestations of toxicity were leucopenia, thrombocytopenia and anemia. Nausea and vomiting are common adverse reactions. Symptoms can be improved by continuous infusion for a long time, or antiemetic agents can be used 24 to 48 hours before treatment. Other toxic effects were diarrhea, neuromuscular disorders, fever, hypotension and rash. The preparation is freshly prepared 3-4h before use.
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CAS:350-46-9
Molecular Formula:C6H4FNO2
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P-Fluoronitrobenzene; 4-Fluornitrobenzol; 1-Fluor-4-Nitrobenzol; Fluoronitrobenzene; 4-Fluoro-1-Nitrobenzene; P-Fluoromitrobenzene; 4-Fluoro-Nitro-Benzene; 4-Nitrofluorobenzene; 1-Fluoro-4-Nitrobenzene; P-Fluoronitorobenzene; Para-Fluoronitrobenzene; P-Nitrofluorobenzene; Para-Nitro Fluorobenzene
Brief Introduction
P-Fluoronitrobenzene is a structural unit of aryl fluorination and a common intermediate for the synthesis of many industrially useful compounds. It can be used to prepare new soluble aromatic polyimides and to synthesize tropisetron.
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CAS:3543-75-7
Molecular Formula:C16H22Cl3N3O2
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Treanda; Cytostasan; Cytostasanhcl; Bendamustinum; Bendamustin Hydrochloride; Bendamustin Hcl; Bendamustinhydrochlorid; Zimet-33/93; Ribomustin; Bendamustine Hydrochloride Hydrate; 4-(5-(Bis(2-Chloroethyl)Amino)-1-Methyl-1H-Benzo[D]Imidazol-2-Yl)Butanoic Acid Hydrochloride
Brief Introduction
Bendamostine hydrochloride was first developed by ozegowski and his colleagues in the microbial experimental Association in Jena, Germany in the early 1860s. The initial purpose was to connect an alkylated nitrogen mustard (a non effective alkylating agent) with a purine and an amino acid. Compared with nitrogen mustard phenylbutyrate, the main advantage of the newly synthesized compound is its water solubility. It was widely used, but until the end of the cold war, the drug has been carried out in Europe for many single drugs or other drugs for the treatment of various hematological malignancies or non Hodgkin's lymphoma, multiple myeloma, CLL and breast cancer. The clinical effect is very significant, significantly reducing the rate of recurrence and mortality, and has little side effects. Good security. So far, bendamostine hydrochloride single drug or combined treatment has been designated as the first-line or second-line treatment option for a variety of hematological malignancies by European and American clinical guidelines.
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CAS:36082-50-5
Molecular Formula:C4HBrCl2N2
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2,4-Dichloro-5-Bromo Pyrimidine
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