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About This Item
线性分子式:
CH3OC6H4SO2Cl
CAS号:
分子量:
206.65
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
推荐产品
品質等級
化驗
96%
折射率
n20/D 1.5560 (lit.)
密度
1.460 g/mL at 25 °C (lit.)
SMILES 字串
COc1cccc(c1)S(Cl)(=O)=O
InChI
1S/C7H7ClO3S/c1-11-6-3-2-4-7(5-6)12(8,9)10/h2-5H,1H3
InChI 密鑰
JHJKSEKUZNJKGO-UHFFFAOYSA-N
應用
3-Methoxybenzenesulfonyl chloride may be used to synthesize 3-(4-phenylpiperazin-1yl) sulfonyls and N-(1-(4-methoxybenzyl)-3-cyclopropyl-1Hpyrazol-5-yl)-3-methoxybenzenesulfonamide.
訊號詞
Danger
危險聲明
危險分類
Eye Dam. 1 - Skin Corr. 1B
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Addressing cytotoxicity of 1, 4-biphenyl amide derivatives: Discovery of new potent and selective 17b-hydroxysteroid dehydrogenase type 2 inhibitors.
Gargano EM, et al.
Bioorganic & Medicinal Chemistry Letters (2015)
Hanumegowda Raju et al.
Recent patents on anti-cancer drug discovery, 6(2), 186-195 (2011-01-21)
In search of synthetic chemotherapeutic substances capable of inhibiting, retarding, or reversing the process of multistage carcinogenesis, we synthesised a series of novel 1-(4-methoxybenzyl)-3-cyclopropyl-1H-pyrazol-5-amine derivatives 9(a-h) by a nucleophilic substitution reaction and characterized by (1)H and (13)C nuclear magnetic resonance
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