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Merck
CN

SRA1

Sigma-Aldrich

甲氧基苯甲醛 溶液

≥97.5% purity (GC), liquid

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MDL编号:
UNSPSC代码:
12171500
PubChem化学物质编号:
NACRES:
NA.47

描述

Spray reagent

质量水平

检测方案

≥97.5% (GC)

形式

liquid

应用

diagnostic assay manufacturing
hematology
histology

储存温度

room temp

SMILES字符串

[H]C(C1=CC=C(OC)C=C1)=O

InChI

1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3

InChI key

ZRSNZINYAWTAHE-UHFFFAOYSA-N

基因信息

human ... CYP1A2(1544)

应用

Excellent reagent for detecting a wide variety of natural products on TLC plates: steroids, prostaglandins, carbohydrates, phenols, glycosides, sapogenins, antibiotics, mycotoxins, antioxidants, etc. A range of colors is produced on heating, adding a qualitative aspect to the detection process.

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2 - Met. Corr. 1 - Skin Irrit. 2 - STOT SE 1

靶器官

Eyes,Central nervous system

WGK

WGK 2

闪点(°F)

52.0 °F

闪点(°C)

11.1 °C

法规信息

危险化学品

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saturation transfer MRI
Annon Bar
Nature (2013)
Jork, H., et al.
Thin Layer Chromatography: Reagents and Detection Methods, 195-198 (1990)
Yun-Hai Tao et al.
Bioorganic & medicinal chemistry letters, 16(3), 592-595 (2005-11-18)
4-Hydroxybenzaldehyde (HBA) derivatives were examined as inhibitors for GABA transaminase (GABA-T) and succinic semialdehyde dehydrogenase (SSADH). Investigation of structure-activity relation revealed that a carbonyl group or an amino group as well as a hydroxy group at the para position of
Li Liu et al.
Bioorganic & medicinal chemistry letters, 22(1), 154-163 (2011-12-06)
The binding between the estrogen receptor α (ER-α) and a variety of compounds in traditional Chinese formulae, Si-Wu-Tang (SWT) series decoctions, was studied using a stably-transfected human breast cancer cell line (MVLN). In 38 compounds tested from SWT series decoctions
Chao-Bin Xue et al.
Bioorganic & medicinal chemistry, 15(5), 2006-2015 (2007-01-30)
Phenoloxidase (PO), also known as tyrosinase, is a key enzyme in insect development, responsible for catalyzing the hydroxylation of tyrosine into o-diphenols and the oxidation of o-diphenols into o-quinones. Inhibition of PO may provide a basis for novel environmentally friendly

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