Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

266477

Sigma-Aldrich

Methyl 4-(hydroxymethyl)benzoate

98%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
HOCH2C6H4CO2CH3
CAS Number:
6908-41-4
Molecular Weight:
166.17
EC Number:
230-017-0
MDL number:
MFCD00009984
UNSPSC Code:
12352100
PubChem Substance ID:
24856142
NACRES:
NA.22

Assay

98%

form

solid

mp

47-50 °C (lit.)

solubility

chloroform: 25 mg/mL, clear, colorless to faint yellow or tan

functional group

ester

SMILES string

COC(=O)c1ccc(CO)cc1

InChI

1S/C9H10O3/c1-12-9(11)8-4-2-7(6-10)3-5-8/h2-5,10H,6H2,1H3

InChI key

VBWFYEFYHJRJER-UHFFFAOYSA-N

Related Categories

Application

Methyl 4-(hydroxymethyl)benzoate was used in the synthesis of keto acid.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
74296PMV
74296PM
01821CH
24630EE
14920EZ

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Stefania Colarusso et al.
Bioorganic & medicinal chemistry letters, 12(4), 705-708 (2002-02-15)
N-terminal truncation of the hexapeptide ketoacid 1 gave rise to potent tripeptide inhibitors of the hepatitis C virus NS3 protease/NS4A cofactor complex. Optimization of these tripeptides led to ketoacid 30 with an IC50 of 0.38 microM. The SAR of these

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service