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244740

Methyl 4-formylbenzoate

Name: Methyl 4-formylbenzoate
Brand: ALDRICH

99%

Synonym(s):

Methyl benzaldehyde-4-carboxylate, Methyl terephthalaldehydate

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About This Item

Linear Formula:

HCOC₆H₄CO₂CH₃

CAS Number:

1571-08-0

Molecular Weight:

164.16

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24854699

EC Number:

216-385-5

Beilstein/REAXYS Number:

775895

MDL number:

MFCD00006950

Assay:

99%

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Properties

Quality Level

200

assay

99%

bp

265 °C (lit.)

mp

59-63 °C (lit.)

functional group

aldehyde, ester

SMILES string

[H]C(=O)c1ccc(cc1)C(=O)OC

InChI

1S/C9H8O3/c1-12-9(11)8-4-2-7(6-10)3-5-8/h2-6H,1H3

InChI key

FEIOASZZURHTHB-UHFFFAOYSA-N

Description

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Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

262.4 °F

flash_point_c

128 °C

ppe

Eyeshields, Gloves, type N95 (US)

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Organocatalysis by bimacrocyclic NHCs: unexpected formation of a cyclic hemiacetal instead of a gamma-butyrolactone.

Ole Winkelmann et al.

Organic & biomolecular chemistry, 7(3), 553-556 (2009-01-22)

Two bimacrocyclic imidazolinium salts of different size, precursors to respective NHCs (N-heterocyclic carbenes), were tested as precatalysts in the reaction of aromatic aldehydes or ketones with enals. The expected lactones were produced in most cases, but in the reaction of

Synthesis and discovery of high affinity folate receptor-specific glycinamide ribonucleotide formyltransferase inhibitors with antitumor activity.

Yijun Deng et al.

Journal of medicinal chemistry, 51(16), 5052-5063 (2008-08-06)

6-Substituted classical pyrrolo[2,3-d]pyrimidine antifolates with a three- to six-carbon bridge between the heterocycle and the benzoyl-L-glutamate (compounds 2-5, respectively) were synthesized starting from methyl 4-formylbenzoate and a Wittig reaction with the appropriate triphenylphosphonium bromide, followed by reduction and conversion to

Two-Dimensional Metal-Organic Framework/Enzyme Hybrid Nanocatalyst as a Benign and Self-Activated Cascade Reagent for in Vivo Wound Healing.

Xinping Liu et al.

ACS nano, 13(5), 5222-5230 (2019-04-20)

Metal-organic frameworks (MOFs)-based peroxidase mimics have been seldom applied in the biomedical field, especially in vivo. One of the main reasons is their optimum reactions occur in strong acidic environments with a pH of 3-4, severely limiting their applications in

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Global Trade Item Number

SKU	GTIN
244740-5G	04061825770017
244740-25G	04061825770000