4-クロマノン

Chromanone

HCID 68110CAS 491-37-2

基本情報

標準SMILES
O=C1CCOc2ccccc21
InChIKey
MSTDXOZUKAQDRL-UHFFFAOYSA-N
分子式
C9H8O2
平均分子量
148.16 g/mol
単同位体質量
148.05242949

名称と識別子

優先名称
Chromanone
IUPAC
2,3-dihydrochromen-4-one
現地名
4-クロマノン
英語名
4-Chromanone
分子式
C9H8O2
分子量
148.16

名称と別名

4-Chromanone491-37-2Chromanone4H-1-Benzopyran-4-one, 2,3-dihydro-2,3-dihydrochromen-4-oneDTXSID3060081RefChem:98630DTXCID1040667CHEBI:38763207-736-3Chroman-4-one2,3-Dihydro-1-benzopyran-4-one
名称をさらに表示
4-クロマノン3,4-ジヒドロ-2H-1-ベンゾピラン-4-オン2H-1-ベンゾピラン-4(3H)-オンクロマン-4-オン2,3-ジヒドロ-4H-1-ベンゾピラン-4-オン4‐クロマノン4-クロマノン, 98+%クロマノン, 4-4-chormanone4-ChlomanoneCHROMANONE, 4-4-Chromanone,99%4-Chromanone >
2,3-Dihydro-4H-chromen-4-one3,4-dihydro-2H-1-benzopyran-4-oneMFCD000068401341-36-22,3-DIHYDRO-4H-1-BENZOPYRAN-4-ONEIsochromanoneEINECS 207-736-3dihydrochromone

データベース識別子

CAS
491-37-2
PubChem CID
68110
DTXSID
DTXSID3060081
ChEMBL
CHEMBL453987
ChEBI
CHEBI:180567
EC Number
207-736-3
Nikkaji
J11.757I

物性

構造計算による物性

XLogP
1.4
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
0
重原子数
11

物理化学的性質

融点
35 · 35-38 °C(lit.)
沸点
127 · 127-128 °C13 mm Hg(lit.)
比重(密度)
1.1291 · 1.1291
屈折率
20 · n20/D 1.575(lit.)
闪点
230 °F · >230 °F
貯蔵温度
Keep in dark place,Sealed in dry,Room Temperature

化学的性質

化学的特性white to light yellow crystal powder

安全と法規制

安全データ

wgk
2
tsca
TSCA listed
rtecs
DJ2981225
hs_code
29329990
risk_code
33-36/37/38
hazard_code
Xi

化学と産業

応用分野

用途有機合成原料。

使用4-Chromanone has been used to study the substrate specificity and catalytic ability of 4-hydroxyacetophenone monooxygenase isolated from Pseudomonas fluorescens ACB

調製方法 · 1 件

純化方法It has been recrystallised from pet ether, or purified by dissolving in *C6H6 washing with H2O, drying (MgSO4), evaporating and distilling in a vacuum, then recrystallising the residue. The liquid has a pleasant lemon-like odour. The semicarbazone has m 227o. [Loudon & Razdan J Chem Soc 4299 1954.] The oxime is prepared from 3g of chromanone, 3g NH2OH.HCl in EtOH (50mL), 6g K2CO3 and refluxed on a water bath for 6hours. The solution is poured into H2O, the solid is filtered off, dried and dissolved in hot *C6H6 which on addition of pet ether yields the oxime as glistening needles m 140o. Hydrolysis of this gives very pure chromanone. The benzal derivative is prepared from 3g of chromanone and 4g PhCHO in 50mL EtOH, heated to boiling, 10mL of conc HCl are added dropwise and set aside for several days. The derivative separates and is recrystallised from EtOH to give yellow needles, m 112o [Powell J Am Chem Soc 45 2711 1923]. Reaction with Pb(OAc)4 yields the 3-acetoxy derivative m 74o (from pet ether + trace of EtOAc) [Cavill et al. J Chem Soc 4573 1954, Beilstein 17/10V 14].

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関連反応

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