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238082

Sigma-Aldrich

4-丁氧基苯甲醛

98%

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About This Item

线性分子式:
CH3(CH2)3OC6H4CHO
CAS号:
5736-88-9
分子量:
178.23
EC號碼:
227-247-9
MDL號碼:
MFCD00003389
分類程式碼代碼:
12352100
PubChem物質ID:
24854289
NACRES:
NA.22

品質等級

100

化驗

98%

形狀

liquid

折射率

n20/D 1.539 (lit.)

bp

285 °C (lit.)

密度

1.031 g/mL at 25 °C (lit.)

SMILES 字串

CCCCOc1ccc(C=O)cc1

InChI

1S/C11H14O2/c1-2-3-8-13-11-6-4-10(9-12)5-7-11/h4-7,9H,2-3,8H2,1H3

InChI 密鑰

XHWMNHADTZZHGI-UHFFFAOYSA-N

相关类别

一般說明

Kinetic constant for the inhibition of the diphenolase activity of mushroom tyrosinase by 4-butoxybenzaldehyde has been evaluated.

應用

4-Butoxybenzaldehyde has been used in the synthesis of:
  • 6-amino-4-(4-butoxyphenyl)-3,5-dicyanopyridine-2(1H)-thione
  • 16-(p-butoxybenzylidene)androsta-1,4-diene-3,17-dione via condensation reaction with androsta-1,4-diene-3,17-dione

法律資訊

储存时变暗对纯度无影响

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

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

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

>235.4 °F - closed cup

閃點（°C）

> 113 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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16-(p-Butoxybenzylidene) androsta-1, 4-diene-3, 17-dione.
Ogawa K, et al.
Acta Crystallographica Section C, Crystal Structure Communications, 48(7), 1359-1361 (1992)
Michael reaction in synthesis of 6-amino-4-(4-butoxyphenyl)-3, 5-dicyanopyridine-2 (1H)-thione.
Dyachenko VD and Litvinov VP.
Chemistry of Heterocyclic Compounds, 34(2), 188-194 (1998)
Dalila Rocco et al.
Molecules (Basel, Switzerland), 24(9) (2019-05-12)
The preparation of 24-functionalized 12,22:26,32-terpyridines (4'-functionalized 3,2:6',3''-terpyridines) by the reaction of three 4-alkoxybenzaldehydes with 3-acetylpyridine and ammonia was investigated; under identical reaction conditions, two (R = nC4H9, C2H5) gave the expected products whereas a third (R = nC3H7) gave only
M Jiménez et al.
Journal of agricultural and food chemistry, 49(8), 4060-4063 (2001-08-22)
A kinetic study of the inhibition of mushroom tyrosinase by 4-substituted benzaldehydes showed that these compounds behave as classical competitive inhibitors, inhibiting the oxidation of L-3,4-dihydroxyphenylalanine (L-DOPA) by mushroom tyrosinase (o-diphenolase activity). The kinetic parameter (K(I)) characterizing this inhibition was
Naoko Ueno et al.
Langmuir : the ACS journal of surfaces and colloids, 33(22), 5393-5397 (2017-05-16)
We evaluated the speed profile of self-propelled underwater oil droplets comprising a hydrophobic aldehyde derivative in terms of their diameter and the surrounding surfactant concentration using a microfluidic device. We found that the speed of the oil droplets is dependent

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