Methyl DL-mandelate, 97%

Name: Methyl DL-mandelate, 97% | 4358-87-6
Brand: J&K Chemical
SKU: JK249289_25_G
Price: 38.8 USD
Availability: OutOfStock

Cat. No JK249289_25_G

Vendor: J&K Chemical

Product Information

Product Name

Methyl DL-mandelate, 97%

Brand Name

J&K

Product Number

249289

CAS

4358-87-6

Molecular Formula

C9H10O3

Molecular Weight

166.17

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

Methyl phenylglycolate

PubChem CID

78066

IUPAC Name

methyl 2-hydroxy-2-phenylacetate

InChI Key

ITATYELQCJRCCK-UHFFFAOYSA-N

SMILES

COC(=O)C(C1=CC=CC=C1)O

Properties

Melting Point

54-56

Boiling Point

135

Flash Point

113

References Data Source From Pubchem

Chiral Separations by Using Capillary Electrochromatography: An Overview

Publication Name: Methods in molecular biology (Clifton, N.J.)

Publication Date: 2026

DOI: 10.1007/978-1-0716-5023-3_23

A Sequence-Based Approach Reveals a Novel Family IV Lipolytic Enzyme in Cereibacter sphaeroides 2.4.1

Publication Name: Molecular Biotechnology

Publication Date: 2025-11-22

DOI: 10.1007/s12033-025-01531-4

Nitrate-induced aerobic oxidative cleavage and esterification of carbon-carbon triple bonds

Publication Name: Science China Chemistry

Publication Date: 2025-06-27

DOI: 10.1007/s11426-025-2711-3

Zirconium Oxide Nanoparticles Catalysed Chemo Selective Reduction of α-Keto Esters and Amides

Publication Name: Topics in Catalysis

Publication Date: 2025-06-10

DOI: 10.1007/s11244-025-02100-4

Synthetic control of chiral pore surfaces in covalent organic frameworks for enantioselective separation of chiral drugs

Publication Name: Science China Chemistry

Publication Date: 2025-01-03

DOI: 10.1007/s11426-024-2452-x

Methyl DL-mandelate, 97%

Product Information

General Information

Properties

References Data Source From Pubchem

Chiral Separations by Using Capillary Electrochromatography: An Overview

A Sequence-Based Approach Reveals a Novel Family IV Lipolytic Enzyme in Cereibacter sphaeroides 2.4.1

Nitrate-induced aerobic oxidative cleavage and esterification of carbon-carbon triple bonds

Zirconium Oxide Nanoparticles Catalysed Chemo Selective Reduction of α-Keto Esters and Amides

Synthetic control of chiral pore surfaces in covalent organic frameworks for enantioselective separation of chiral drugs