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Merck

550779

Sigma-Aldrich

2-碘苯甲醛

97%

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About This Item

线性分子式:
IC6H4CHO
CAS号:
分子量:
232.02
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

mp

36-39 °C (lit.)

官能基

aldehyde
iodo

儲存溫度

2-8°C

SMILES 字串

Ic1ccccc1C=O

InChI

1S/C7H5IO/c8-7-4-2-1-3-6(7)5-9/h1-5H

InChI 密鑰

WWKKTHALZAYYAI-UHFFFAOYSA-N

相关类别

一般說明

2-Iodobenzaldehyde (o-iodobenzaldehyde) is a 2-halobenzaldehyde derivative. Its crystals belong to the orthorhombic crystal system and P212121 space group.

應用

2-Iodobenzaldehyde may be used as a reactant in the synthesis of the following heterocycles:
  • 2,3-diaryl-1-indenones
  • indolo[1,2-a]quinazolines
  • Baylis-Hillman (BH) adducts
It may also be used in preparing:
  • 5-phenylindazolo[3,2-b]quinazolin-7(5H)-one
  • 4-(3-iodophenyl)-2,2:6,2-terpyridine
  • fluoren-9-one
  • 2-formyl-3′-methoxybiphenyl

象形圖

Exclamation mark

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


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分析证书(COA)

Lot/Batch Number

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其他客户在看

Slide 1 of 1

1 of 1

Copper (I)-Catalyzed Synthesis of 5-Arylindazolo [3, 2-b] quinazolin-7 (5 H)-one via Ullmann-Type Reaction
Chen DS, et al.
The Journal of Organic Chemistry, 78(11), 5700-5704 (2013)
A simple copper-catalyzed two-step one-pot synthesis of indolo [1, 2-a] quinazoline.
Li C, et al.
Beilstein Journal of Organic Chemistry, 10(1), 2441-2447 (2014)
Ring-Closing Olefin Metathesis of 2, 2'-Divinylbiphenyls: A Novel and General Approach to Phenanthrenes.
Iuliano A, et al.
Organic Letters, 6(21), 3711-3714 (2004)
2-Iodobenzaldehyde.
Betz R and Klufers P.
Acta Crystallographica Section E, Structure Reports Online, 63(12), o4879-o4879 (2007)
Synthesis of indanones via intramolecular Heck reaction of Baylis-Hillman adducts of 2-iodobenzaldehyde.
Park JB, et al.
Bull. Korean Chem. Soc., 25(6), 927-930 (2004)

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