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[ CAS No. 90-64-2 ] {[proInfo.proName]}

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Chemical Structure| 90-64-2
Chemical Structure| 90-64-2
Structure of 90-64-2 * Storage: {[proInfo.prStorage]}

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Product Citations

Kaili Yan ; Morgan L. Huddleston ; Brett A. Gerdes , et al. DOI:

Abstract: Electrochemical conversion of biomass-derived intermediate compounds to high-value products has emerged as a promising approach in the field of biorefinery. Biomass upgrading allows for the production of chemicals from non-fossil-based carbon sources and capitalization on electricity as a green energy input. Amino acids, as products of biomass upgrading, have received relatively little attention. Pharmaceutical and food industries will benefit from an alternative strategy for the production of amino acids that does not rely on inefficient fermentation processes. The use of renewable biomass resources as starting materials makes this proposed strategy more desirable. Herein, we report an electrochemical approach for the selective oxidation of biomass-derived α-hydroxyl acids to α-keto acids, followed by electrochemical reductive amination to yield amino acids as the final products. Such a strategy takes advantage of both reactions at the anode and cathode and produces amino acids under ambient conditions with high energy efficiency. A flow electrolyzer was also successfully employed for the conversion of α-hydroxyl acids to amino acids, highlighting its great potential for large-scale application.

Purchased from AmBeed: ; ; ; ; 56-40-6 ; 156-06-9 ; ; ; 298-12-4 ; ; ; ; 828-01-3 ;

Product Details of [ 90-64-2 ]

CAS No. :90-64-2 MDL No. :MFCD00064250
Formula : C8H8O3 Boiling Point : -
Linear Structure Formula :(C6H5)CH(OH)CO2H InChI Key :IWYDHOAUDWTVEP-UHFFFAOYSA-N
M.W : 152.15 Pubchem ID :1292
Synonyms :
DL-Mandelic acid;(±)-Mandelic acid;DL-Amygdalic Acid
Chemical Name :2-Hydroxy-2-phenylacetic acid

Calculated chemistry of [ 90-64-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 39.15
TPSA : 57.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.79 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.99
Log Po/w (XLOGP3) : 0.62
Log Po/w (WLOGP) : 0.48
Log Po/w (MLOGP) : 0.78
Log Po/w (SILICOS-IT) : 0.76
Consensus Log Po/w : 0.73

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -1.45
Solubility : 5.45 mg/ml ; 0.0358 mol/l
Class : Very soluble
Log S (Ali) : -1.4
Solubility : 6.02 mg/ml ; 0.0396 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.23
Solubility : 9.02 mg/ml ; 0.0593 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.59

Safety of [ 90-64-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338-P310 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:
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