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244740

Sigma-Aldrich

Methyl 4-formylbenzoate

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
Beilstein:
775895
EC Number:
216-385-5
MDL number:
MFCD00006950
UNSPSC Code:
12352100
PubChem Substance ID:
24854699
NACRES:
NA.22

Assay

99%

bp

265 °C (lit.)

mp

59-63 °C (lit.)

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

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Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

262.4 °F

Flash Point(C)

128 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

244740-VAR:
244740-25G:
244740-1G:
244740-BULK:
244740-5G:

Certificates of Analysis (COA)

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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
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
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
Naoya Kishikawa et al.
Phytochemical analysis : PCA, 29(1), 112-117 (2017-09-13)
Tanshinones are a major class of bioactive ingredients in the traditional herbal medicines, Danshen (Salvia miltiorrhiza). A sensitive and reliable determination method for tanshinones is useful to ensure the quality of Danshen. To develop a sensitive and selective analytical method
Mahmoud Elcheikh Mahmoud et al.
Journal of the American Chemical Society, 141(17), 7115-7121 (2019-04-12)
In this study, we report the successful incorporation of the photoactive bis(4'-(4-carboxyphenyl)-terpyridine)ruthenium(II) (Ru(cptpy)2) strut into a robust metal-organic framework (MOF), AUBM-4. The single crystal X-ray analysis revealed the formation of a new one-dimensional structure of Ru(cptpy)2 complexes linked together by Zr
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