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Merck
CN

499749

Sigma-Aldrich

2-苄氧基苯甲醛

98%

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About This Item

线性分子式:
C6H5CH2OC6H4CHO
CAS号:
分子量:
212.24
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

98%

折射率

n20/D 1.6 (lit.)

沸点

326 °C (lit.)

密度

1.339 g/mL at 25 °C (lit.)

SMILES字符串

O=Cc1ccccc1OCc2ccccc2

InChI

1S/C14H12O2/c15-10-13-8-4-5-9-14(13)16-11-12-6-2-1-3-7-12/h1-10H,11H2

InChI key

PBEJTRAJWCNHRS-UHFFFAOYSA-N

一般描述

2-苄氧基苯甲醛是苯甲醛衍生物。在存在钒 (V) 手性salen配合物和咪唑的情况下,它与氰基甲酸乙酯发生对映选择性氰甲基化反应,形成相应的氰醇碳酸酯。

应用

2-苄氧基苯甲醛可用于合成:
  • 2-苄氧基-2′-羟基-3′,4′,6′-三甲氧查耳酮
  • N2-(2-苄氧基)亚苄基异烟酸酰肼。
  • 2-羟基-2′-甲氧基二苯甲酮
  • 2′-羟基-5,6,7-三甲氧基黄酮

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The synthesis of 5, 2'-dihydroxy-6, 8-dimethoxyflavone and its isomers: A revised structure of skullcapflavone I.
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Synthesis and structure-activity relationship of cytotoxic 5,2',5'-trihydroxy-7,8-dimethoxyflavanone analogues.
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Michael J Hearn et al.
European journal of medicinal chemistry, 44(10), 4169-4178 (2009-06-16)
Structural modification of the frontline antitubercular isonicotinic acid hydrazide (INH) provides lipophilic adaptations (3-46) of the drug in which the hydrazine moiety of the parent compound has been chemically blocked from the deactivating process of N(2)-acetylation by N-arylaminoacetyl transferases. As

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