167037
3-甲基水杨酸
96.0%
别名:
2-羟基-3-甲基苯甲酸, 邻甲基水杨酸
登录 查看组织和合同定价。
选择尺寸
关于此项目
线性分子式:
CH3C6H3(OH)CO2H
化学文摘社编号:
分子量:
152.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-473-8
Beilstein/REAXYS Number:
2086811
MDL number:
产品名称
3-甲基水杨酸, 96.0%
InChI key
WHSXTWFYRGOBGO-UHFFFAOYSA-N
InChI
1S/C8H8O3/c1-5-3-2-4-6(7(5)9)8(10)11/h2-4,9H,1H3,(H,10,11)
SMILES string
Cc1cccc(C(O)=O)c1O
assay
96.0%
mp
163-165 °C (lit.)
solubility
methanol: soluble 5%, clear to slightly hazy (colorlessto faint brown)
正在寻找类似产品? 访问 产品对比指南
Application
3-甲基水杨酸可用于合成：
- 8-甲基-2-硫代-2-3,3-二氢-4H-1,3-苯并恶嗪-4-酮
- 7-羟基-8-甲基-2-硫代-2-3,3-二氢-4H-1,3-苯并恶嗪-4-酮
- (R)-, (S)-和(RS)-羟甲基美西汀
General description
3-甲基水杨酸可与WOCl4反应生成氧化水杨酸钨（VI）络合物。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Krithika Delhiraja et al.
Environmental monitoring and assessment, 192(7), 432-432 (2020-06-17)
Emerging contaminants (ECs) have become an increasing area of concern due to the likely impacts of these compounds on human health and the environment. Generally, products which are used for households and personal care activities contribute to major percentage of
Generalized Method for the Production of 1, 3-Benzoxazine, 1, 3-Benzothiazine, and Quinazoline Derivatives from 2-(Hydroxy, Thio, or Amino) Aromatic Acids Using Triphenylphosphine Thiocyanogen.
Pritchard KM, et al.
Synthetic Communications, 35(!2), 1601-1611 (2005)
Synthesis of (R)-, (S)-, and (RS)-hydroxymethylmexiletine, one of the major metabolites of mexiletine.
Cavalluzzi MM, et al.
Tetrahedron Asymmetry, 18(20), 2409-2417 (2007)
Thais Kroetz et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 18(5), 1171-1184 (2019-02-28)
In this article, new fluorescent lipophilic based benzazoles were synthesized from the reaction between photoactive formyl derivatives and aliphatic amines followed by NaBH4 reduction with good yields. The photophysics of the benzazoles was investigated experimentally and theoretically. These compounds present
On structure-related properties of synthetic organic clot-dissolving (thrombolytic) compounds.
K N von Kaulla et al.
Biochemical pharmacology, 16(6), 1023-1034 (1967-06-01)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持