所有图片(1)

文件

252794

3-羟基苯甲酸甲酯

Name: 3-羟基苯甲酸甲酯
Brand: ALDRICH

99%

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别名:

3-(Methoxycarbonyl)phenol, 3-Carbomethoxyphenol, 3-Hydroxybenzoic acid methyl ester, Methyl m-hydroxybenzoate, m-Carbomethoxyphenol, m-Hydroxybenzoic acid methyl ester

线性分子式:

HOC₆H₄CO₂CH₃

CAS号:

19438-10-9

分子量:

152.15

Beilstein:

2208129

EC 号:

243-071-5

MDL编号:

MFCD00002295

PubChem化学物质编号:

24855238

NACRES:

NA.22

检测方案

99%

形式

solid

bp

280-281 °C/709 mmHg (lit.)

mp

70-72 °C (lit.)

SMILES string

COC(=O)c1cccc(O)c1

InChI

1S/C8H8O3/c1-11-8(10)6-3-2-4-7(9)5-6/h2-5,9H,1H3

InChI key

YKUCHDXIBAQWSF-UHFFFAOYSA-N

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应用

Methyl 3-hydroxybenzoate has been used in synthesis of:

3-hydroxybenzene-1,2-dicarbaldehyde
O-methyl O-[3-methyl-4-(methylthio)phenyl]O-(3-methylcarboxyphenyl) phosphorothioate

象形图

GHS07

警示用语：

Warning

危险声明

H302 - H315 - H319 - H335

预防措施声明

P261 - P264 - P271 - P301 + P312 - P302 + P352 - P305 + P351 + P338

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

分析证书(COA)

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示例

T1503

货号

25G

包装规格/数量

其它示例：

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

输入内容 1.000309185)

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Investigation of the effect of hapten heterology on immunoassay sensitivity and development of an enzyme-linked immunosorbent assay for the organophosphorus insecticide fenthion.

Kim YJ, et al.

Analytica Chimica Acta, 94(1, 29-40 (2003)

Structural elucidation and synthesis of 3-hydroxybenzene-1,2-dicarbaldehyde from astigmatid mites.

T Sakata et al.

Bioscience, biotechnology, and biochemistry, 65(10), 2315-2317 (2002-01-05)

The structure of a novel aromatic compound contained in the unidentified Rhizoglyhus mite (Acaridae: Astigmata) was elucidated, without its isolation, to be 3-hydroxybenzene-1,2-dicarbaldehyde (tentatively named gamma-acaridial) by a combination of GC/MS and GC/FT-IR together with knowledge of related mite compounds.

Discovery of a previously unknown biosynthetic capacity of naringenin chalcone synthase by heterologous expression of a tomato gene cluster in yeast.

Deze Kong et al.

Science advances, 6(44) (2020-11-01)

Chalcone synthase (CHS) canonically catalyzes carbon-carbon bond formation through iterative decarboxylative Claisen condensation. Here, we characterize a previously unidentified biosynthetic capability of SlCHS to catalyze nitrogen-carbon bond formation, leading to the production of a hydroxycinnamic acid amide (HCAA) compound. By

Synthesis and Comparative Structure-Activity Study of Carbohydrate-Based Phenolic Compounds as α-Glucosidase Inhibitors and Antioxidants.

Shota Machida et al.

Molecules (Basel, Switzerland), 24(23) (2019-12-01)

Twenty-one natural and unnatural phenolic compounds containing a carbohydrate moiety were synthesized and their structure-activity relationship (SAR) was evaluated for α-glucosidase inhibition and antioxidative activity. Varying the position of the galloyl unit on the 1,5-anhydro-d-glucitol (1,5-AG) core resulted in changes

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