Chemicals list & Research Gallery

N-Methylimidazole
CAS number: 616-47-7
N-Methylimidazole is a 1H-imidazole having a methyl substituent at the N-1 position.
Representation of the numbering used throughout the paper for the Meim and Mepym ligands: N-Methylimidazole, 4-methylpyrimidine.
Representation of the numbering used throughout the paper for the Meim and Mepym ligands: N-Methylimidazole, 4-methylpyrimidine.
N-Acetyl-L-Cysteine
CAS number: 616-91-1
N-acetyl-L-cysteine is an N-acetyl-L-amino acid that is the N-acetylated derivative of the natural amino acid L-cysteine. It has a role as an antiinfective agent, an antioxidant, an antiviral drug, an antidote to paracetamol poisoning, a vulnerary, a mucolytic, a human metabolite, a radical scavenger, a ferroptosis inhibitor and a geroprotector. It is a L-cysteine derivative, an acetylcysteine and a N-acetyl-L-amino acid. It is a conjugate acid of a N-acetyl-L-cysteinate.
Concentration of N-acetylcysteine in the aqueous phase with time during a normal peroxidation experiment using antioxidant 16a.
Concentration of N-acetylcysteine in the aqueous phase with time during a normal peroxidation experiment using antioxidant 16a.
4-Iodobenzoic acid
CAS number: 619-58-9
4-Iodobenzoic acid is a white crystalline solid and is essentially a derivative of benzoic acid with an iodine substituent.
Initial Screening of P-C Coupling of 4-Iodobenzoic Acid under Conventional Heating
Initial Screening of P-C Coupling of 4-Iodobenzoic Acid under Conventional Heating
4-Nitrobenzoic acid
CAS number: 62-23-7
4-nitrobenzoic acid is a nitrobenzoic acid having the nitro group at the 4-position. It is functionally related to a benzoic acid.
Effect of reaction solvent on the kinetic parameters of the aldol reaction of 2a with 1a in the presence of 20 mol % 3a and p-nitrobenzoic acid.
Effect of reaction solvent on the kinetic parameters of the aldol reaction of 2a with 1a in the presence of 20 mol % 3a and p-nitrobenzoic acid.
Aniline
CAS number: 62-53-3
Aniline is a clear to slightly yellow liquid with a characteristic odor. It does not readily evaporate at room temperature.
(A) Ligation of AOB to phage-displayed aldehydes is accelerated by aniline, but preincubation of phage with aniline in the absence of AOB leads to rapid loss of aldehyde and loss of reactivity toward AOB. (B) In anilinium acetate, pH 4.7, the aldehyde disappears with t1/2 ∼40 min; however, aldehydes alone are stable at the same pH in sodium acetate buffer.
(A) Ligation of AOB to phage-displayed aldehydes is accelerated by aniline, but preincubation of phage with aniline in the absence of AOB leads to rapid loss of aldehyde and loss of reactivity toward AOB. (B) In anilinium acetate, pH 4.7, the aldehyde disappears with t1/2 ∼40 min; however, aldehydes alone are stable at the same pH in sodium acetate buffer.
Scope of aniline partners 2b–2j.
Scope of aniline partners 2b–2j.
Cinnamic acid
CAS number: 621-82-9
Cinnamic acid is a monocarboxylic acid that consists of acrylic acid bearing a phenyl substituent at the 3-position. It is found in Cinnamomum cassia.
Topochemical [2 + 2] photodimerization of cinnamic acids.
Topochemical [2 + 2] photodimerization of cinnamic acids.
Coronatine
CAS number: 62251-96-1
Coronatine is a N-acyl-amino acid.
Structures of coronatine (+)-1, jasmonic acid (-)-4, and their derivatives.
Structures of coronatine (+)-1, jasmonic acid (-)-4, and their derivatives.
Retrosynthesis of coronatine and their stereoisomers. A: Retrosynthesis of coronatine and their derivatives. B: Retrosynthesis of coronamic acid moieties.
Retrosynthesis of coronatine and their stereoisomers. A: Retrosynthesis of coronatine and their derivatives. B: Retrosynthesis of coronamic acid moieties.
Synthesis of naturally occurring coronatine (+)-1 and stereoisomers (-)-1, (+)-7, and (-)-7. aEnantio excess was calculated by chiral HPLC analysis.
Synthesis of naturally occurring coronatine (+)-1 and stereoisomers (-)-1, (+)-7, and (-)-7. aEnantio excess was calculated by chiral HPLC analysis.
Effects of synthetic coronatines and related compounds on stomatal aperture in epidermis of I. tricolor (A) and a stoma in epidermis of I. tricolor (B).
Effects of synthetic coronatines and related compounds on stomatal aperture in epidermis of I. tricolor (A) and a stoma in epidermis of I. tricolor (B).
Coronafacic acid
CAS number: 62251-98-3
Coronafacic acid (CFA) is the polyketide component of the phytotoxin coronatine, a virulence factor of the plant pathogen Pseudomonas syringae.
Structures of coronatine (+)-1, jasmonic acid (-)-4, and their derivatives.
Structures of coronatine (+)-1, jasmonic acid (-)-4, and their derivatives.
Synthesis of coronafacic acid ( )-2. The product was obtained as a Et3N salt.
Synthesis of coronafacic acid ( )-2. The product was obtained as a Et3N salt.
4-Chloroanisole
CAS number: 623-12-1
4-Chloroanisole is an electron-rich chloroarene.
Cross-coupling reactions of 4-chloroanisole in THF at 60 °C were performed using various derivatives of SPhos.
Cross-coupling reactions of 4-chloroanisole in THF at 60 °C were performed using various derivatives of SPhos.
Cross-coupling reaction of a deactivated substrate, p-chloroanisole (12), and sodium phenyltrihydroxyborate mediated by complex 11 in air.
Cross-coupling reaction of a deactivated substrate, p-chloroanisole (12), and sodium phenyltrihydroxyborate mediated by complex 11 in air.
Thermal profile of the reaction of p-chloroanisole (12) and sodium phenyltrihydroxyborate in air mediated by complex 11.
Thermal profile of the reaction of p-chloroanisole (12) and sodium phenyltrihydroxyborate in air mediated by complex 11.
Ethyl cyanoformate
CAS number: 623-49-4
Ethyl cyanoformate is a colorless to pale yellow liquid, known for its reactivity in organic synthesis, particularly as a cyanating agent. It's used in various reactions, including the introduction of cyanide groups into organic molecules and the synthesis of β-cyano-substituted acrylates.
Cyanation of various aldehydes (4) with ethyl cyanoformate (3) catalyzed by DMA
Cyanation of various aldehydes (4) with ethyl cyanoformate (3) catalyzed by DMA
Cyanation of various ketones (8) with ethyl cyanoformate (3) catalyzed by DMA
Cyanation of various ketones (8) with ethyl cyanoformate (3) catalyzed by DMA