推荐产品
等級
SAJ first grade
蒸汽密度
4.7 (vs air)
蒸汽壓力
100 mmHg ( 17.8 °C)
105 mmHg ( 20 °C)
化驗
≥90.0%
形狀
liquid
存貨情形
available only in Japan
折射率
n20/D 1.443 (lit.)
bp
68-70 °C (lit.)
mp
−54 °C (lit.)
密度
1.665 g/mL at 20 °C (lit.)
SMILES 字串
ClS(Cl)(=O)=O
InChI
1S/Cl2O2S/c1-5(2,3)4
InChI 密鑰
YBBRCQOCSYXUOC-UHFFFAOYSA-N
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訊號詞
Danger
危險聲明
危險分類
Acute Tox. 2 Inhalation - Eye Dam. 1 - Skin Corr. 1C - STOT SE 3
標靶器官
Respiratory system
安全危害
儲存類別代碼
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
水污染物質分類（WGK）
WGK 1
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Manli Zhang et al.
Chemical communications (Cambridge, England), 47(41), 11522-11524 (2011-09-29)
A palladium-catalyzed direct desulfitative C-arylation of a benzo[d]oxazole C-H bond with arene sulfonyl chlorides is described. The procedure tolerates halo, cyano, nitro, trifluoromethyl, acetyl and acetylamino groups on the phenyl ring of sulfonyl chlorides, providing the arylation products in moderate
Philippe Hermange et al.
Organic letters, 11(18), 4044-4047 (2009-08-15)
Reaction of an isoquinoline, a silyloxyfuran, and an acyl or sulfonyl chloride provides easy access to a wide variety of isoquinolinobutyrolactones with excellent yields and diastereoselectivites (R*,R* isomer), even in the case of formation of quaternary centers (i.e., R(3) or
Qian Wu et al.
Chemical communications (Cambridge, England), 47(32), 9188-9190 (2011-07-14)
A new, efficient protocol for the synthesis of di(hetero)aryl sulfides is described. Cheap and easily available arylsulfonyl chlorides as a sulfur source reductively couple with electron-rich (hetero)arenes (e.g., indolizines, indoles, electron-rich benzenes, etc.) in the presence of triphenylphosphine to afford
Ourida Saidi et al.
Journal of the American Chemical Society, 133(48), 19298-19301 (2011-11-04)
A selective catalytic meta sulfonation of 2-phenylpyridines was found to occur in the presence of (arene)ruthenium(II) complexes upon reaction with sulfonyl chlorides. The 2-pyridyl group facilitates the formation of a stable Ru-C(aryl) σ bond that induces a strong para-directing effect.
Tandem cyclizations of 1,6-enynes with arylsulfonyl chlorides by using visible-light photoredox catalysis.
Guo-Bo Deng et al.
Angewandte Chemie (International ed. in English), 52(5), 1535-1538 (2013-01-05)
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