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3-Hydroxyphenylacetic acid - 10mM in DMSO, high purity , CAS No.621-37-4
Basic Description
Synonyms
3-Hydroxyphenylacetic acid | 621-37-4 | 2-(3-hydroxyphenyl)acetic acid | (3-Hydroxyphenyl)acetic acid | 3-Hydroxybenzeneacetic acid | (m-Hydroxyphenyl)acetic acid | Benzeneacetic acid, 3-hydroxy- | M-HYDROXYPHENYLACETIC ACID | 3-Hydroxyphenylacetate | Acetic acid, (m-hydro
Specifications & Purity
10mM in DMSO
Storage Temp
Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description
3-Hydroxyphenylacetic Acid (cas# 621-37-4) is a compound useful in organic synthesis
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Phenols
Subclass
1-hydroxy-4-unsubstituted benzenoids
Intermediate Tree Nodes
Not available
Direct Parent
1-hydroxy-4-unsubstituted benzenoids
Alternative Parents
1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as 1-hydroxy-4-unsubstituted benzenoids. These are phenols that are unsubstituted at the 4-position.
External Descriptors
monocarboxylic acid - phenols
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
2-(3-hydroxyphenyl)acetic acid
INCHI
InChI=1S/C8H8O3/c9-7-3-1-2-6(4-7)5-8(10)11/h1-4,9H,5H2,(H,10,11)
InChIKey
FVMDYYGIDFPZAX-UHFFFAOYSA-N
Smiles
C1=CC(=CC(=C1)O)CC(=O)O
Isomeric SMILES
C1=CC(=CC(=C1)O)CC(=O)O
WGK Germany
3
Molecular Weight
152.15
Reaxy-Rn
2086506
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2086506&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Melt Point(°C)
129-133°C
Molecular Weight
152.150 g/mol
XLogP3
0.900
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
2
Exact Mass
152.047 Da
Monoisotopic Mass
152.047 Da
Topological Polar Surface Area
57.500 Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
144.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Bing Wang, RuiQing Zhang, HuiYong Chen, Zhuo Li, EnZhou Liu, HaiXia Ma, Bo Zhou, Hong Hao, LinYu Jiao.
(2023)
Construction of supramolecular S-scheme heterojunctions assisted by hydrogen bond subtle-tuning actuates highly efficient photocatalytic oxidation.
CHEMICAL ENGINEERING JOURNAL,
473
(145290).
2.
Xinyi Zhang, Jiakun Zhou, Zemin Li, Yimin Qin, Ruitao Yu, Huaiwei Zhang, Yuhong Zheng, Jiangwei Zhu, Demeng Zhang, Li Fu.
(2019)
The Qualitative Electrochemical Determination of Multiple Components in Seaweed Fertilizer.
International Journal of Electrochemical Science,
14
(6283).
3.
Hui-Ying Wang, Cheng Qu, Meng-Ning Li, Chao-Ran Li, Run-Zhou Liu, Zifan Guo, Ping Li, Wen Gao, Hua Yang.
(2022)
Time-Series-Dependent Global Data Filtering Strategy for Mining and Profiling of Xenobiotic Metabolites in a Dynamic Complex Matrix: Application to Biotransformation of Flavonoids in the Extract of Ginkgo biloba by Gut Microbiota.
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,
70
(45):
(14386–14394).
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