Home Other Building Blocks 2-Hydroxy-2-(4-hydroxyphenyl)acetic acid

2-Hydroxy-2-(4-hydroxyphenyl)acetic acid

CAS No.:
1198-84-1
Catalog Number:
AG000POM
Molecular Formula:
C8H8O4
Molecular Weight:
168.1467
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$32
- +
25g
98%
In Stock USA
United States
$94
- +
100g
98%
In Stock USA
United States
$225
- +
500g
98%
In Stock USA
United States
$900
- +
Product Description
Catalog Number:
AG000POM
Chemical Name:
2-Hydroxy-2-(4-hydroxyphenyl)acetic acid
CAS Number:
1198-84-1
Molecular Formula:
C8H8O4
Molecular Weight:
168.1467
MDL Number:
MFCD00004234
IUPAC Name:
2-hydroxy-2-(4-hydroxyphenyl)acetic acid
InChI:
InChI=1S/C8H8O4/c9-6-3-1-5(2-4-6)7(10)8(11)12/h1-4,7,9-10H,(H,11,12)
InChI Key:
YHXHKYRQLYQUIH-UHFFFAOYSA-N
SMILES:
OC(=O)C(c1ccc(cc1)O)O
Properties
Complexity:
160  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
168.042g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
168.148g/mol
Monoisotopic Mass:
168.042g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
77.8A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
0.3  
Literature
Title Journal
Halicloic acids A and B isolated from the marine sponge Haliclona sp. collected in the Philippines inhibit indoleamine 2,3-dioxygenase. Journal of natural products 20120824
A public resource for metabolic pathway mapping of Aspergillus fumigatus Af293. Medical mycology 20110401
Metabolic engineering of the L-phenylalanine pathway in Escherichia coli for the production of S- or R-mandelic acid. Microbial cell factories 20110101
The metabolic fate of red wine and grape juice polyphenols in humans assessed by metabolomics. Molecular nutrition & food research 20100701
The rate-limiting catalytic steps of hydroxymandelate synthase from Amycolatopsis orientalis. Biochemistry 20100309
Investigation into the mechanism of phenolic couplings during the biosynthesis of glycopeptide antibiotics. Chembiochem : a European journal of chemical biology 20080922
Two roads diverged: the structure of hydroxymandelate synthase from Amycolatopsis orientalis in complex with 4-hydroxymandelate. Biochemistry 20080219
The genome of the versatile nitrogen fixer Azorhizobium caulinodans ORS571. BMC genomics 20080101
Adaptogenic and nootropic activities of aqueous extract of Vitis vinifera (grape seed): an experimental study in rat model. BMC complementary and alternative medicine 20050101
Engineering p-hydroxyphenylpyruvate dioxygenase to a p-hydroxymandelate synthase and evidence for the proposed benzene oxide intermediate in homogentisate formation. Biochemistry 20040127
Improved chemical strategies for the targeted therapy of cancer. Angewandte Chemie (International ed. in English) 20031013
Structure, biosynthetic origin, and engineered biosynthesis of calcium-dependent antibiotics from Streptomyces coelicolor. Chemistry & biology 20021101
Properties