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Merck
CN

553581

Sigma-Aldrich

6-溴-2-羟基-3-甲氧基苯甲醛

98%

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About This Item

线性分子式:
BrC6H2(OH)(OCH3)CHO
CAS号:
分子量:
231.04
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

98%

mp

102-105 °C (lit.)

SMILES字符串

COc1ccc(Br)c(C=O)c1O

InChI

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

InChI key

JUPJZUTYDWXZAQ-UHFFFAOYSA-N

一般描述

6-Bromo-2-hydroxy-3-methoxybenzaldehyde is a bromobenzaldehyde derivative. It participates in the synthesis of (±)-norannuradhapurine. Its crystals exhibit monoclinic crystal system and space group P21/n.

应用

6-Bromo-2-hydroxy-3-methoxybenzaldehyde may be used in the synthesis of:
  • 2-benzyloxy-6-bromo-3-methoxybenzaldehyde
  • biphenyls
  • antihypertensive natural products S-(+)-XJP and R-(-)-XJP

象形图

Exclamation mark

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

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分析证书(COA)

Lot/Batch Number

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访问文档库

Total synthesis and the biological activities of (?)-norannuradhapurine.
Nimgirawath S, et al.
Molecules (Basel), 14(1), 89-101 (2008)
Synthetic studies on selective adenosine A 2A receptor antagonists: Synthesis and structure-activity relationships of novel benzofuran derivatives
Saku O, et al.
Bioorganic & Medicinal Chemistry Letters, 20(3), 1090-1093 (2010)
First total synthesis of antihypertensive natural products S-(+)-XJP and R-(-)-XJP.
Wang C, et al.
Organic & Biomolecular Chemistry, 12(37), 7338-7344 (2014)
The conformation of some ortho-bromoarylaldehydes.
Hanson JR, et al.
J. Chem. Res. (M), 7, 416-418 (2008)
Synthesis of NK109, an anticancer benzo [c] phenanthridine alkaloid.
Nakanishi T, et al.
The Journal of Organic Chemistry, 63(13), 4235-4239 (1998)

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