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Home > Other Building Blocks > 23255-59-6
23255-59-6 | Benzoic acid, 2-hydroxy-6-[2-(4-hydroxyphenyl)ethyl]-
CAS No: 23255-59-6 Catalog No: AG002MP4 MDL No:
Product Description
Catalog Number:
AG002MP4
Chemical Name:
Benzoic acid, 2-hydroxy-6-[2-(4-hydroxyphenyl)ethyl]-
CAS Number:
23255-59-6
Molecular Formula:
C15H14O4
Molecular Weight:
258.2693
IUPAC Name:
2-hydroxy-6-[2-(4-hydroxyphenyl)ethyl]benzoic acid
InChI:
InChI=1S/C15H14O4/c16-12-8-5-10(6-9-12)4-7-11-2-1-3-13(17)14(11)15(18)19/h1-3,5-6,8-9,16-17H,4,7H2,(H,18,19)
InChI Key:
GFSQDOUEUWXRSL-UHFFFAOYSA-N
SMILES:
Oc1ccc(cc1)CCc1cccc(c1C(=O)O)O
UNII:
9ZQ3FYV21C
Properties
Complexity:
297
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
258.089g/mol
Formal Charge:
0
Heavy Atom Count:
19
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
3
Isotope Atom Count:
0
Molecular Weight:
258.273g/mol
Monoisotopic Mass:
258.089g/mol
Rotatable Bond Count:
4
Topological Polar Surface Area:
77.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.5
Literature
| Title | Journal |
|---|---|
| Genomewide analysis of carotenoid cleavage dioxygenases in unicellular and filamentous cyanobacteria. | Comparative and functional genomics 20120101 |
| Evolutionarily conserved regulatory mechanisms of abscisic acid signaling in land plants: characterization of ABSCISIC ACID INSENSITIVE1-like type 2C protein phosphatase in the liverwort Marchantia polymorpha. | Plant physiology 20100301 |
| [Chemical constituents of fresh celery]. | Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20090601 |
| Design and evaluation of anacardic acid derivatives as anticavity agents. | European journal of medicinal chemistry 20080601 |
| Molecular design of anti-MRSA agents based on the anacardic acid scaffold. | Bioorganic & medicinal chemistry 20070915 |
| Directed ortho-metalation of unprotected benzoic acids. Methodology and regioselective synthesis of useful contiguously 3- and 6-substituted 2-methoxybenzoic acid building blocks. | Organic letters 20060216 |
| Inhibition of endothelial cell functions by novel potential cancer chemopreventive agents. | Biochemical and biophysical research communications 20041203 |
| Stilbenecarboxylate biosynthesis: a new function in the family of chalcone synthase-related proteins. | Phytochemistry 20030201 |
| The biological and structural similarity between lunularic acid and abscisic acid. | Bioscience, biotechnology, and biochemistry 20020401 |
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