所有图片(2)
About This Item
线性分子式:
lC6H3(OH)CHO
CAS号:
分子量:
248.02
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
97%
mp
98-100 °C (lit.)
官能团
aldehyde
iodo
SMILES字符串
Oc1ccc(I)cc1C=O
InChI
1S/C7H5IO2/c8-6-1-2-7(10)5(3-6)4-9/h1-4,10H
InChI key
PDFVIWFKGYODKD-UHFFFAOYSA-N
相关类别
一般描述
5-Iodosalicylaldehyde is a salicylaldehyde derivative.
应用
5-Iodosalicylaldehyde may be used to synthesize:
- 5-formylsalicylaldehyde
- 5-ortho-carboranylsalicylaldehyde
- new salen (N,N′-Bis(salicylidene)ethylenediamine) ligands that are tethered to a p-acylthio(phenylacetylene)n linker
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
Synthesis of 5-ortho-Carboranylsalicylaldehyde and an Indolinospirobenzopyran.
Lee SH, et al.
Synthetic Communications, 39(22), 4069-4078 (2009)
Synthesis and catalytic properties of p-acylthio (phenylacetylene) n substituted chiral manganese salen complexes.
Nielsen M and Gothelf KV.
Journal of the Chemical Society. Perkin Transactions 1, 19 (2001)
An efficient and convenient synthesis of 5-formylsalicylaldehyde.
Lee SH, et al.
Synthetic Communications, 30(6), 1003-1008 (2000)
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