1571-08-0 | Methyl 4-formylbenzoate

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$13.00	$9.00
100g	98%	in stock	$36.00	$25.00

Description

• Catalog Number: AA79136
• Chemical Name: Methyl 4-formylbenzoate
• CAS Number: 1571-08-0
• Molecular Formula: C9H8O3
• Molecular Weight: 164.158
• MDL Number: MFCD00006950
• SMILES: COC(=O)c1ccc(cc1)C=O
• NSC Number: 28459

Computed Properties

• Complexity: 169
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• XLogP3: 1.7

Literature

• Bis{μ-(E)-methyl 4-[(2-carbamothio-ylhydrazinyl-idene)meth-yl]benzoate-κS:S}bis-[iodido(triphenyl-phosphane-κP)copper(I)].

  Acta crystallographica. Section E, Structure reports online 20111101

• 4-Carbomethoxybenzaldehyde as a highly sensitive pre-column fluorescence derivatization reagent for 9,10-phenanthrenequinone.

  Talanta 20110715

• N-silyl oxyketene imines are underused yet highly versatile reagents for catalytic asymmetric synthesis.

  Nature chemistry 20101101

• Methyl 4-(1H-benzimidazol-2-yl)benzoate trihydrate.

  Acta crystallographica. Section E, Structure reports online 20101101

• Shoot differentiation from protocorm callus cultures of Vanilla planifolia (Orchidaceae): proteomic and metabolic responses at early stage.

  BMC plant biology 20100101

• Potent and selective inhibitors of breast cancer resistance protein (ABCG2) derived from the p-glycoprotein (ABCB1) modulator tariquidar.

  Journal of medicinal chemistry 20090226

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

  Organic & biomolecular chemistry 20090207

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

  Journal of medicinal chemistry 20080828

• Factors affecting the selectivity of the oxidation of methyl p-toluate by cobalt(III).

  Inorganic chemistry 20080317

• Synthesis and GIAO NMR calculations for some new 4,5-dihydro-1H-1,2,4-triazol-5-one derivatives: comparison of theoretical and experimental 1H and 13C chemical shifts.

  Magnetic resonance in chemistry : MRC 20050701

• Solid-phase synthesis of 1-substituted tetrahydroisoquinoline derivatives employing BOC-protected tetrahydroisoquinoline carboxylic acids.

  Journal of combinatorial chemistry 20040101

• The preparation of a series of nitrostilbene ester compounds using micro reactor technology.

  The Analyst 20010101