推薦產品
化驗
98%
形狀
powder
mp
112-114 °C (lit.)
SMILES 字串
NNC(=O)c1ccccc1
InChI
1S/C7H8N2O/c8-9-7(10)6-4-2-1-3-5-6/h1-5H,8H2,(H,9,10)
InChI 密鑰
WARCRYXKINZHGQ-UHFFFAOYSA-N
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訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Oral - Carc. 2 - Skin Irrit. 2
儲存類別代碼
13 - Non Combustible Solids
水污染物質分類（WGK）
WGK 3
個人防護裝備
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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[reaction: see text] An isoniazid-NAD adduct has been recently proposed as the ultimate metabolite responsible for the antituberculous activity of isoniazid (INH). Its structure results from binding of the isonicotinoyl radical at C4 position of the nicotinamide ring of NAD
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Journal of inorganic biochemistry, 99(3), 876-882 (2005-02-15)
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Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(3), 486-496 (2011-05-03)
A systematic vibrational spectroscopic assignment and analysis of benzohydrazide (BH) has been carried out by using FTIR and FT-Raman spectral data. The vibrational analysis were aided by electronic structure calculations--ab initio (RHF) and hybrid density functional methods (B3LYP and B3PW91)
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