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About This Item
线性分子式:
SnCl2 · 2H2O
CAS号:
分子量:
225.65
EC號碼:
MDL號碼:
分類程式碼代碼:
12161600
PubChem物質ID:
NACRES:
NA.22
推荐产品
等級
ACS reagent
化驗
≥99.99% trace metals basis
反應適用性
core: tin
reagent type: catalyst
bp
652 °C (lit.)
652 °C
mp
37-38 °C (dec.) (lit.)
正離子痕跡
Ca: ≤0.005%
Fe: ≤0.003%
K: ≤0.005%
Na: ≤0.01%
Pb: ≤0.01%
SMILES 字串
O.O.Cl[SnH2]Cl
InChI
1S/2ClH.2H2O.Sn/h2*1H;2*1H2;/q;;;;+2/p-2
InChI 密鑰
FWPIDFUJEMBDLS-UHFFFAOYSA-L
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相关类别
應用
还原剂；羰基烯丙基化反应；路易斯酸催化剂，用于C-C键形成反应；以AgClO4为催化剂，合成α-糖苷；烯烃、二烯、顺式-乙烯基环氧乙烷和烯丙基硒化物的合成；1,4-内过氧化物的脱氧反应；作为1,3-二噻烷，保护羧酸；选择性对甲氧基苄基醚裂解试剂；加氢甲酰化和羰基化反应的添加剂。
特點和優勢
符合 A.C.S. 试剂规范。
訊號詞
Danger
危險分類
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT RE 2 Oral - STOT SE 3
標靶器官
Cardio-vascular system, Respiratory system
儲存類別代碼
8B - Non-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
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
其他客户在看
David J Hallett et al.
Organic & biomolecular chemistry, 10(30), 6130-6158 (2012-04-20)
Reactions of the allyltin trichloride 45 generated from (4S)-4-benzyloxypent-2-enyl(tributyl)stannane 1 with imines prepared from glyoxylates proceed with useful levels of 1,5-stereocontrol in favour of (4E)-2,6-anti-2-(alkylamino)-6-benzyloxyhept-4-enoates 49. This stereoselectivity, controlled by the chirality of the stannane, dominates over any intrinsic stereochemical
Grégory Dupeyre et al.
Organic & biomolecular chemistry, 9(22), 7780-7790 (2011-10-07)
A six-step one-pot reaction was designed for synthesizing homodimeric 7-phenylindolo[3,2-a]carbazoles from 1H-indoles and β-nitrostyrenes, in the presence of SnCl(2)·2H(2)O. The reactions proceeded under very mild conditions and the desired heterocycles were obtained in moderate to good yields. An unprecedented mechanism
Olivier Germay et al.
Organic & biomolecular chemistry, 10(48), 9709-9733 (2012-11-17)
The tin(IV) chloride mediated cyclisation of (Z)-homoallylic alcohols using phenylselenenyl chloride or phthalimide in the presence of a Lewis acid followed by reductive removal of the phenylselenenyl group was found to give 2,5-cis-disubstituted tetrahydrofurans with excellent stereocontrol. Using this procedure
Aili Sun et al.
Talanta, 88, 259-264 (2012-01-24)
The Zn-Sn nanoparticles/multiwall carbon nanotubes (Zn-SnNPs/MWNTs) nanocomposite film was prepared by electrodeposition of ZnCl(2) and SnCl(2) on MWNTs simultaneously in Ethaline ionic liquids. Then, based on immobilizing hemoglobin (Hb) within a novel Zn-SnNPs/MWNTs nanocomposite film (Hb/Zn-SnNPs/MWNTs), a novel hydrogen peroxide
Rajendran Suresh et al.
The Journal of organic chemistry, 77(3), 1468-1476 (2012-01-11)
The synthesis of 2-(1H-pyrrolo[2,3-b]pyridin-3-yl)quinolines by a SnCl(2)-catalyzed multicomponent reaction has been described. The reaction proceeds chemo- and regioselectively in an atom-economic way, generating a library of 24 quinoline derivatives.
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