m-アニスアルデヒド

3-Methoxybenzaldehyde

HCID 11569CAS 591-31-1

基本情報

標準SMILES
COc1cccc(C=O)c1
InChIKey
WMPDAIZRQDCGFH-UHFFFAOYSA-N
分子式
C8H8O2
平均分子量
136.15 g/mol
単同位体質量
136.0524295

概要

3-methoxybenzaldehyde is a member of the class of benzaldehydes in which the hydrogen at position 3 of benzaldehyde has been replaced by a methoxy group. It has a role as a Brassica napus metabolite. It is a member of benzaldehydes and a monomethoxybenzene.

名称と識別子

優先名称
3-Methoxybenzaldehyde
IUPAC
3-methoxybenzaldehyde
現地名
m-アニスアルデヒド
英語名
3-Methoxybenzaldehyde
分子式
C8H8O2
分子量
136.15

名称と別名

3-Methoxybenzaldehyde591-31-13-AnisaldehydeBenzaldehyde, 3-methoxy-MetamethoxybenzaldehydeDTXSID50444478ZAO7S0IVHNSC-43794DTXCID3024447CHEBI:136805RefChem:94623209-712-8
名称をさらに表示
m-アニスアルデヒド1-ホルミル-3-メトキシベンゼンm-メトキシベンズアルデヒド3-メトキシベンズアルデヒド1-メトキシ-3-ホルミルベンゼン3-アニスアルデヒド3-メトキシベンゼンカルボアルデヒドmアニスアルデヒドmメトキシベンズアルデヒドM‐アニスアルデヒド3-メトキシベンズアルデヒド, 98%3-methoxy-benzaldehyd3-methoxybenzaldehdem-AnisaLANISALDEHYDE,3-META-ANISALDEHYD
M-ANISALDEHYDEm-Methoxybenzaldehyde3-Methoxy-benzaldehydeMFCD00003361CCRIS 960META-ANISALDEHYDEEINECS 209-712-8UNII-8ZAO7S0IVH

データベース識別子

CAS
591-31-1
PubChem CID
11569
DTXSID
DTXSID5044447
ChEMBL
CHEMBL22585
ChEBI
CHEBI:136805
UNII
8ZAO7S0IVH
EC Number
209-712-8
Nikkaji
J6.757A

物性

構造計算による物性

XLogP
1.8
極性表面積
26.3 Ų
水素結合供与体数
0
水素結合受容体数
2
回転可能結合数
2
重原子数
10

実験および物理化学的性質

SpringerMaterials Properties13C nuclear magnetic resonance spectrum
LogP1.710
Flavoring AgentsEU Flavoring substances
Boiling Point143.00 °C. @ 50.00 mm Hg
Physical DescriptionLiquid

物理化学的性質

融点
187 °C · 187 °C
沸点
143 °C50 · 143 °C50 mm Hg(lit.)
比重(密度)
1.117 g/mL · 1.117 g/mL at 20 °C(lit.)
蒸気圧
1.3 hPa · 1.3 hPa (73 °C)
屈折率
20 · n20/D 1.553(lit.)
闪点
230 °F · >230 °F

化学的性質

化学的特性clear pale yellow to yellow liquid. Soluble in ethanol, diethyl ether, and benzene; insoluble in water.

安全と法規制

GHS分類

GHS Classification · 5 件

This chemical does not meet GHS hazard criteria for 6% (5 of 84) of reports.

Warning

H315 (94%): Causes skin irritation [Warning Skin corrosion/irritation]

P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 84 reports by companies from 10 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Regulatory Information · 3 件

Chemical: Benzaldehyde, 3-methoxy-

Commission Regulation (EC) No 1565/2000 (Repealed by Com. Implementing Reg. (EU) No 872/2012)

Benzaldehyde, 3-methoxy-: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationEvaluation - Chemicals not considered for in depth evaluation - Not commercially active in Australia
Hazard Classes and CategoriesSkin Irrit. 2 (94%)

安全データ

F
9-23
wgk
3
tsca
TSCA listed
rtecs
BZ2605000
毒性
sce-hmn:lyms 1 mmol/L MUREAV 206,17,88
hs_code
29124900

化学と産業

薬理情報

Cellular LocationsCytoplasm

用途と製造

General Manufacturing InformationBenzaldehyde, 3-methoxy-: INACTIVE
応用分野 · 3 件

用途トリフェニルメタン系酸性染料の中間体。

使用3-Methoxybenzaldehyde is used to prepare 3-(3-methoxy-phenyl)-1-phenyl-propenone by reaction with benzldehyde. It is used as an eluent for mono-13C isotopomers of vanillin in normal phase silica gel chromatography. It acts as an inhibitor of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) metabolism.

一般的な説明m-Anisaldehyde has significant antifungal activity against Candida sp., including the azole-resistant strains.

調製方法

製造方法3-Methoxybenzaldehyde is obtained by the reaction of m-hydroxybenzaldehyde and dimethyl sulfate.

純化方法Wash it with saturated aqueous NaHCO3, then H2O, dry it with anhydrous MgSO4 and distil it under reduced pressure under N2. Store it under N2 in sealed glass ampoules. [Beilstein 8 IV 241.]

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