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About This Item
线性分子式:
(O2N)2C6H3SO2Cl
CAS号:
分子量:
266.62
Beilstein:
2147583
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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化驗
97%
形狀
solid
mp
101-103 °C (lit.)
官能基
nitro
SMILES 字串
[O-][N+](=O)c1ccc(c(c1)[N+]([O-])=O)S(Cl)(=O)=O
InChI
1S/C6H3ClN2O6S/c7-16(14,15)6-2-1-4(8(10)11)3-5(6)9(12)13/h1-3H
InChI 密鑰
SSFSNKZUKDBPIT-UHFFFAOYSA-N
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一般說明
2,4-二硝基苯磺酰氯引起糖胺发生磺化，产生 N-糖基-2,4-二硝基苯磺酰胺。
可能含有高达 3.5％ 的苯
應用
2,4-二硝基苯磺酰氯用于保护伯胺。它在合成 2-[（（2,4-二硝基苯基）磺酰基]氨基乙酸叔丁酯中用作起始试剂。
訊號詞
Danger
危險分類
Carc. 1A - Eye Dam. 1 - Muta. 1B - Skin Corr. 1B - STOT RE 2
標靶器官
Blood
儲存類別代碼
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
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
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Vishwanath Gaitonde et al.
Journal of carbohydrate chemistry, 31(4-6), 353-370 (2013-01-26)
The N-glycosyl-2,4-dinitrobenzenesulfonamides were accessed via benzoyl-protected β-glycosyl azides. The azides were reduced with Adams' catalyst to the corresponding amines. The glycosylamines were sulfonated with 2,4-dinitrobenzenesulfonyl chloride to form N-glycosyl-2,4-dinitrobenzenesulfonamides in moderate yields. β-Glycosyl amides were then prepared in 67 -
Rachel J Ball et al.
Artificial DNA, PNA & XNA, 1(1), 27-35 (2011-06-21)
Halogen-labelled peptide organic acid (HPOA) monomers have been synthesised and incorporated into sequence-specific peptide nucleic acid (PNA) probes. Three different types of probe have been prepared; the unmodified PNA probe, the PNA probe with a mass marker, and the PNA
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