所有图片(2)
About This Item
线性分子式:
lC6H3(OH)CHO
CAS号:
分子量:
248.02
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%
mp
98-100 °C (lit.)
SMILES 字串
Oc1ccc(I)cc1C=O
InChI
1S/C7H5IO2/c8-6-1-2-7(10)5(3-6)4-9/h1-4,10H
InChI 密鑰
PDFVIWFKGYODKD-UHFFFAOYSA-N
相关类别
一般說明
5-Iodosalicylaldehyde is a salicylaldehyde derivative.
應用
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
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
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
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
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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