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Merck
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478075

Sigma-Aldrich

2-溴-3-羟基-4-甲氧基苯甲醛

97%

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About This Item

線性公式:
BrC6H2(OH)(OCH3)CHO
CAS號碼:
分子量::
231.04
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

mp

202-207 °C (lit.)

SMILES 字串

COc1ccc(C=O)c(Br)c1O

InChI

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

InChI 密鑰

QPDFBPIHEDAUKK-UHFFFAOYSA-N

相關類別

一般說明

2-Bromo-3-hydroxy-4-methoxybenzaldehyde, also known as 2-bromo-isovanillin, can be synthesized by the bromination of 3-hydroxy-4-methoxybenzaldehyde.

應用

2-Bromo-3-hydroxy-4-methoxybenzaldehyde (2-Bromo-isovanillin) may be used in the preparation of:
  • 2-hydroxy-3-methoxybenzaldehyde semicarbazone (HMBS)
  • 2-cyclopentyl-7-methoxy-1-benzofuran-4-carbaldehyde
  • 3-(benzyloxy)-2-bromo-4-methoxybenzaldehyde
It may also be used as a starting material in the total synthesis of the following natural products:
  • pareitropone
  • denbinobin
  • (±)-codeine

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


分析證明 (COA)

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Concise syntheses of (-)-galanthamine and (?)-codeine via intramolecular alkylation of a phenol derivative.
Magnus P, et al.
Journal of the American Chemical Society, 131(44), 16045-16047 (2009)
Synthesis and preliminary biological evaluation of novel taspine derivatives as anticancer agents.
Zhang J, et al.
European Journal of Medicinal Chemistry, 45(7), 2798-2805 (2010)
Chemoselective Zinc/HCl Reduction of Halogenated β-Nitrostyrenes: Synthesis of Halogenated Dopamine Analogues.
Maresh JJ, et al.
Synlett, 25, 2891-2894 (2014)
A concise synthesis of denbinobin.
Wang YC, et al.
Tetrahedron Letters, 46(47), 8103-8104 (2005)
Growth, spectral, and thermal characterization of 2-hydroxy-3-methoxybenzaldehyde semicarbazone.
Binil PS, et al.
Journal of Thermal Analysis and Calorimetry, 112(2), 913-919 (2013)

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