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Methyl 3 formylbenzoate

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Methyl-3-formylbenzoate is a chemical compound used in various laboratory applications. It is a colorless, crystalline solid that serves as a precursor or intermediate in organic synthesis. The core function of this product is to provide a source of the 3-formylbenzoate moiety for further chemical transformations and reactions. No additional details or interpretations about its intended use can be provided while maintaining an unbiased and factual approach.

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Lab products found in correlation

N boc 2 aminoacetaldehyde, by Merck Group (2 mentions) 4 methoxybenzaldehyde, by Thermo Fisher Scientific (2 mentions) Imidazole 4 carboxaldehyde, by Thermo Fisher Scientific (2 mentions) 3 phenylpropionaldehyde, by Thermo Fisher Scientific (2 mentions) Boc l alanine aldehyde, by Chem-Impex (2 mentions)

2 protocols using methyl 3 formylbenzoate

1

Synthesis of Chiral Amino Acid Precursors

Check if the same lab product or an alternative is used in the 5 most similar protocols
(R)-Methyl 2-(((benzyloxy) carbonyl)amino)but-3-enoate (lot# DAZ6Z4) and (S)-Methyl 2-(((benzyloxy)carbonyl)amino)but-3-enoate (lot# T1FKZ2) from Aurum Pharmatech LLC (no COA confirming chirality were available). (R)-Methyl 2-(((benzyloxy)carbonyl)amino)but-3-enoate (alpha), (R)-tert-butyl (1-oxopropan-2-yl)carbamate [lot# P105–00984, ([a]D = 7.4°, C = 1 CH3OH), P105–03363 (10.4°, C = 0.68, CH3OH), P102–08388, P165–01932 (([a]D = 9.453° (C = 1 CH3OH)) from Astatech Inc. N-Boc-2-aminoacetaldehyde from Sigma Aldrich, Borane dimethyl sulfide complex, Acetaldehyde 99 %, (1S)-(−)- α Pinene mixture of enantiomers 98 %, Phenylacetaldehyde ≥ 95 %, 4-Methoxybenzaldehyde, Imidazole-4-carboxaldehyde manufactured by Alfa Aesar, methyl-3-formylbenzoate, 3-Phenylpropionaldehyde ≥ 95 %, by Acros Organics were purchased from VWR. 4-formylbenzenesulfonyl chloride, (−)-ɑ-Methoxy-ɑ-(trifluoromethyl)phenylacetyl chloride (Lot# 10210747, optical rotation −136.3° neat) manufactured by Alfa Aesar were purchased from VWR Boc-l-alanine aldehyde ( [a]D20=−37.8° (C = 1.0 in CH3OH)) from Chem-Impex International. N-Boc-l-Phenylalaninal (97 %) (−43.7° (20 °C, 589 nm) (C = 0.5, CH3OH)), N-Boc-d-Phenylalaninal (97 %) (+44° (20 °C, 589 nm) (C = 0.5, CH3OH)) from Acros Organics.
, & Wilpon J.G. (1995). Voice-processing technologies--their application in telecommunications.. Proceedings of the National Academy of Sciences of the United States of America, 92(22), 9991-9998.
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2

Synthesis of Chiral Amino Acid Precursors

Check if the same lab product or an alternative is used in the 5 most similar protocols
(R)-Methyl 2-(((benzyloxy) carbonyl)amino)but-3-enoate (lot# DAZ6Z4) and (S)-Methyl 2-(((benzyloxy)carbonyl)amino)but-3-enoate (lot# T1FKZ2) from Aurum Pharmatech LLC (no COA confirming chirality were available). (R)-Methyl 2-(((benzyloxy)carbonyl)amino)but-3-enoate (alpha), (R)-tert-butyl (1-oxopropan-2-yl)carbamate [lot# P105–00984, ([a]D = 7.4°, C = 1 CH3OH), P105–03363 (10.4°, C = 0.68, CH3OH), P102–08388, P165–01932 (([a]D = 9.453° (C = 1 CH3OH)) from Astatech Inc. N-Boc-2-aminoacetaldehyde from Sigma Aldrich, Borane dimethyl sulfide complex, Acetaldehyde 99 %, (1S)-(−)- α Pinene mixture of enantiomers 98 %, Phenylacetaldehyde ≥ 95 %, 4-Methoxybenzaldehyde, Imidazole-4-carboxaldehyde manufactured by Alfa Aesar, methyl-3-formylbenzoate, 3-Phenylpropionaldehyde ≥ 95 %, by Acros Organics were purchased from VWR. 4-formylbenzenesulfonyl chloride, (−)-ɑ-Methoxy-ɑ-(trifluoromethyl)phenylacetyl chloride (Lot# 10210747, optical rotation −136.3° neat) manufactured by Alfa Aesar were purchased from VWR Boc-l-alanine aldehyde ( [a]D20=−37.8° (C = 1.0 in CH3OH)) from Chem-Impex International. N-Boc-l-Phenylalaninal (97 %) (−43.7° (20 °C, 589 nm) (C = 0.5, CH3OH)), N-Boc-d-Phenylalaninal (97 %) (+44° (20 °C, 589 nm) (C = 0.5, CH3OH)) from Acros Organics.
Nguyen L., Schultz D.C., Terzyan S.S., Rezaei M., Songb J., Li C., You Y, & Hanigan M.H. (2022). Design and evaluation of novel analogs of 2-amino-4-boronobutanoic acid (ABBA) as inhibitors of human gamma-glutamyl transpeptidase. Bioorganic & medicinal chemistry, 73, 116986.
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