跳转至内容
Merck
CN

238082

4-丁氧基苯甲醛

98%

登录 查看组织和合同定价。

选择尺寸

变更视图

关于此项目

线性分子式:
CH3(CH2)3OC6H4CHO
化学文摘社编号:
分子量:
178.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
227-247-9
MDL number:
Assay:
98%
Form:
liquid
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助


Quality Level

assay

98%

form

liquid

refractive index

n20/D 1.539 (lit.)

bp

285 °C (lit.)

density

1.031 g/mL at 25 °C (lit.)

functional group

aldehyde

SMILES string

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 key

XHWMNHADTZZHGI-UHFFFAOYSA-N

General description

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

Application

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

Legal Information

储存时变暗对纯度无影响


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

>235.4 °F - closed cup

flash_point_c

> 113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

新产品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库



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



全球贸易项目编号

货号GTIN
238082-10G04061836683399