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410470

Sigma-Aldrich

5-溴-2-羟基-3-甲氧基苯甲醛

97%

别名:

5-溴-3-甲氧基水杨醛

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About This Item

线性分子式:
BrC6H2(OH)(OCH3)CHO
CAS号:
5034-74-2
分子量:
231.04
MDL號碼:
MFCD00016593
分類程式碼代碼:
12352100
PubChem物質ID:
24865528
NACRES:
NA.22

化驗

97%

形狀

solid

mp

125-127 °C (lit.)

官能基

aldehyde
bromo

SMILES 字串

COc1cc(Br)cc(C=O)c1O

InChI

1S/C8H7BrO3/c1-12-7-3-6(9)2-5(4-10)8(7)11/h2-4,11H,1H3

InChI 密鑰

MMFKBTPDEVLIOR-UHFFFAOYSA-N

相关类别

應用

5-Bromo-2-hydroxy-3-methoxybenzaldehyde may be employed for the following syntheses:
  • ailanthoidol, via Stille coupling
  • 6-bromo-8-methoxy-3-(methoxycarbonyl)-2H-chromen-2-one
  • benzimidazole-based ligand, 2-(1H-benzoimidazol-2-yl)-4-bromo-6-methoxy-phenol (HL)
  • chromogenic reagent, 5-bromo-2-hydroxy-3-methoxybenzaldehyde-p-hydroxy benzoic hydrazone
  • (E)-N′-(5-bromo-2-hydroxy-3-methoxybenzylidene)-2-hydroxybenzohydrazide monohydrate

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

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
BGBB8609
MKBJ8143V
06631AJ
02414HH
11919AH

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Direct Spectrophotometric Determination of Ni (II) Using 5-Bromo-2-hydroxyl-3-methoxybenzaldehyde-4-hydroxy benzoichydrazone.
Saritha B and Reddy TS.
J. Appl. Chem., 7(3), 22-26 (2014)
(E)-N'-(5-Bromo-2-hydroxy-3-methoxybenzylidene)-2-hydroxybenzohydrazide monohydrate.
Zhao S, et al.
Acta Crystallographica Section E, Structure Reports Online, 68(7), 2040-2040 (2012)
Transformation of a luminescent benzimidazole-based Yb3 cluster into a one-dimensional coordination polymer.
Yang X, et al.
Crystal Growth & Design, 10(2), 970-976 (2009)
Shun-Yu Lin et al.
The Journal of organic chemistry, 68(7), 2968-2971 (2003-03-29)
Ailanthoidol 1, which can be isolated from Chinese herbal medicine, is achieved in which the longest linear sequence is only six steps in 48% overall yield from commercially available 5-bromo-2-hydroxy-3-methoxybenzaldehyde. The key transformations in the synthesis are the Stille coupling
Pedro Verdía et al.
Molecules (Basel, Switzerland), 16(6), 4379-4388 (2011-05-31)
The ionic liquid 1,3-dimethylimidazolium methyl sulfate, [MMIm][MSO₄], together with a small amount of water (the amount taken up by the ionic liquid upon exposure to air), acts efficiently as both solvent and catalyst of the Knoevenagel condensation reactions of malononitrile

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