D-4-Methoxymandelic acid, 98%

Name: D-4-Methoxymandelic acid, 98% | 20714-89-0
Brand: J&K Chemical
SKU: JK961701_5_G
Price: 246.5 USD
Availability: OutOfStock

Cat. No JK961701_5_G

Vendor: J&K Chemical

Product Information

Product Name

D-4-Methoxymandelic acid, 98%

Brand Name

J&K

Product Number

961701

CAS

20714-89-0

Molecular Formula

C9H10O4

Molecular Weight

182.17

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

6951708

IUPAC Name

(2R)-2-hydroxy-2-(4-methoxyphenyl)acetic acid

InChI Key

ITECRQOOEQWFPE-MRVPVSSYSA-N

SMILES

COC1=CC=C(C=C1)C@H(C(=O)O)O

Properties

Density

1.309

Boiling Point

370

References Data Source From Pubchem

Deracemization of Racemic α-Hydroxy Acids

Publication Name: Science of Synthesis

Publication Date: 2019

Synthesis of d-Phenylglycines from Racemic Mandelic Acids

Publication Name: Science of Synthesis

Publication Date: 2019

Mandelate Racemase

Publication Name: Science of Synthesis

Publication Date: 2015

Relationships between the racemic structures of substituted mandelic acids containing 8- and 10-membered hydrogen bonded dimer rings

Publication Name: CrystEngComm

Publication Date: 2014

DOI: 10.1039/c4ce01832j

An efficient and practical synthesis of mandelic acid by combination of complex phase transfer catalyst and ultrasonic irradiation

Publication Name: Ultrasonics Sonochemistry

Publication Date: 2008-09

DOI: 10.1016/j.ultsonch.2008.03.001

D-4-Methoxymandelic acid, 98%

Product Information

General Information

Properties

References Data Source From Pubchem

Deracemization of Racemic α-Hydroxy Acids

Synthesis of d-Phenylglycines from Racemic Mandelic Acids

Mandelate Racemase

Relationships between the racemic structures of substituted mandelic acids containing 8- and 10-membered hydrogen bonded dimer rings

An efficient and practical synthesis of mandelic acid by combination of complex phase transfer catalyst and ultrasonic irradiation