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333638

Sigma-Aldrich

4-丙氧基苯甲醛

97%

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About This Item

线性分子式:
CH3CH2CH2OC6H4CHO
CAS号:
5736-85-6
分子量:
164.20
MDL號碼:
MFCD00014134
分類程式碼代碼:
12352100
PubChem物質ID:
24860159

化驗

97%

形狀

liquid

折射率

n20/D 1.546 (lit.)

bp

129-130 °C/10 mmHg (lit.)

密度

1.039 g/mL at 25 °C (lit.)

官能基

aldehyde

SMILES 字串

CCCOc1ccc(C=O)cc1

InChI

1S/C10H12O2/c1-2-7-12-10-5-3-9(8-11)4-6-10/h3-6,8H,2,7H2,1H3

InChI 密鑰

FGXZWMCBNMMYPL-UHFFFAOYSA-N

一般說明

Kinetic constants for the inhibition of the diphenolase activity of mushroom tyrosinase by 4-propoxybenzaldehyde was evaluated.

應用

4-Propoxybenzaldehyde was used in the preparation of (2S,4S,5R)-(±)-2-(4-propoxyphenyl)-3,4-dimethyl-5-phenyl-1,3-oxazolidine via condensation with 1-ephedrine.

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - 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, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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分析证书(COA)

Lot/Batch Number
MKCC3322
MKCB9271
MKBW2084V
MKBP4711V
MKBJ1877V

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C-HO and CH (arene) interactions in (2S, 4S, 5R)-(-)-2-(4-propoxyphenyl)-3, 4-dimethyl-5-phenyl-1, 3-oxazolidine.
Duffy M, et al.
AZo Journal of Materials Online, 60(2), o234-o236 (2004)
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

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