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203440

Sigma-Aldrich

三氯化铟

99.999% trace metals basis

别名:

三氯化铟

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About This Item

线性分子式:
InCl3
CAS号:
10025-82-8
分子量:
221.18
EC號碼:
233-043-0
MDL號碼:
MFCD00011058
分類程式碼代碼:
12352302
PubChem物質ID:
24852172
NACRES:
NA.23
化驗:
99.999% trace metals basis
形狀:
powder or flakes (or chunks)

品質等級

200

化驗

99.999% trace metals basis

形狀

powder or flakes (or chunks)

反應適用性

reagent type: catalyst
core: indium

雜質

≤15.0 ppm Trace Metal Analysis

密度

3.46 g/mL at 25 °C (lit.)

SMILES 字串

Cl[In](Cl)Cl

InChI

1S/3ClH.In/h3*1H;/q;;;+3/p-3

InChI 密鑰

PSCMQHVBLHHWTO-UHFFFAOYSA-K

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相关类别

一般說明

氯化铟是一种路易斯酸催化剂，适于多种有机反应。还用于催化、太阳能电池和光电领域。

應用

氯化铟适于：
  • 作为醛和酮制备1,3-二硫戊环的催化剂。
  • 用于酚、硫醇、醇和胺的酰化。
  • 作为前体制备染料敏化太阳能电池的氧化铟锡(ITO)薄膜。
  • 制备溶液加工的 氧化物半导体薄膜晶体管(OS TFT)用于 显示装置。

象形圖

Health hazardCorrosion
GHS08,GHS05

訊號詞

Danger

危險聲明

H314,H372,H412

危險分類

Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1C - STOT RE 1 Inhalation

標靶器官

Lungs

儲存類別代碼

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials 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

从最新的版本中选择一种：

分析证书(COA)

Lot/Batch Number
MKCQ8460
MKCN1567
MKCM9692
MKCL9420
MKCL5270

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Mecheril Valsan Nandakumar et al.
Chemical communications (Cambridge, England), (26), 2756-2758 (2007-06-28)
The indium-bipyridine-catalyzed, enantioselective ring-opening of meso-epoxides with aliphatic and aromatic thiols furnished 1,2-mercapto alcohols in good yields and excellent enantioselectivities; the crystal structure of the chiral catalyst reveals a pentagonal-bipyramidal coordination geometry around the indium center.
Synthesis, 1712-1712 (2007)
Tetrahedron Letters, 48, 6743-6743 (2007)
Theresa A Proia et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 26(23), 6335-6349 (2020-09-19)
Danvatirsen is a therapeutic antisense oligonucleotide (ASO) that selectively targets STAT3 and has shown clinical activity in two phase I clinical studies. We interrogated the clinical mechanism of action using danvatirsen-treated patient samples and conducted back-translational studies to further elucidate
Naveen Mulakayala et al.
Bioorganic & medicinal chemistry letters, 22(15), 5063-5066 (2012-07-04)
A convenient and practical methodology for the synthesis of 2-aryl quinazolin-4(3H)-ones by the condensation of o-aminobenzamides with aromatic aldehydes under mild conditions using catalytic InCl(3) with good yields and high selectivities. This method has been extended for the synthesis of
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