42348-40-3

Basic information

• Product Name: Benzoic acid, 2-hydroxy-5-nitro-, ethyl ester
• CAS NO: 42348-40-3
• Molecular Formula: C9H9NO5
• Molecular Weight: 211.174
• Mol File: 42348-40-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-hydroxy-5-nitro-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-hydroxy-5-nitro-, ethyl ester(42348-40-3)
• EPA Substance Registry System: Benzoic acid, 2-hydroxy-5-nitro-, ethyl ester(42348-40-3)

Safety Data

• Hazardous Substances Data: 42348-40-3(Hazardous Substances Data)

Upstream product

• 118-61-6 2-hydroxy-benzoic acid ethyl ester 
• 72078-81-0 3,5-dinitro-1-(4-nitro-benzyloxy)-1H-pyridin-2-one 
• 1007476-32-5 sodium ethyl acetylacetate enolate 
• 14150-94-8 3,5-dinitro-1-methyl-2-pyridone 
• 141-97-9 ethyl acetoacetate 
• 618-98-4 ethyl 3-nitrobenzoate 
• 3094-08-4 5-Nitro-2-ethoxy-benzotrifluorid 
• 69-72-7 salicylic acid 
• 181294-58-6 N-tert-butyl-β-formyl-β-nitroenamine 
• 75-03-6 ethyl iodide 
• 96-97-9 5-nitrosalicylic acid 

Downstream Products

• 2912-78-9 2-hydroxy-5-nitrobenzamide 
• 62773-65-3 ethyl 5-amino-2-hydroxybenzoate 
• 86840-93-9 N-n-Butyl-N'-(2-hydroxy-5-nitrobenzoyl)-diaminoethan-1,2 
• 86840-95-1 N-n-Dodecyl-N'-(2-hydroxy-5-nitrobenzoyl)-diaminoethan-1,2 
• 86840-94-0 N-n-Octyl-N'-(2-hydroxy-5-nitrobenzoyl)-diaminoethan-1,2 
• 96-97-9 5-nitrosalicylic acid 
• 155388-71-9 benzyl 2-hydroxy-5-nitrobenzoate 
• 874523-84-9 2-benzyloxy-5-nitrobenzoic acid 
• 337520-12-4 4-(1-t-butoxycarbonylpiperidin-4-yloxy)-3-ethoxycarbonylnitrobenzene 
• 301653-20-3 2-allyloxy-5-nitrobenzoic acid 
• 17794-30-8 ethyl 2-acetoxy-5-nitrobenzoate 
• 1080633-33-5 C₁₄H₁₉NO₅ 
• 1080633-31-3 C₁₇H₂₄N₂O₇ 
• 855749-73-4 2-benzyloxy-5-nitro-benzoic acid ethyl ester 

Relevant articles and documents

Photocatalytic Selective Reduction by TiO2 of 5-Nitrosalicylic Acid Ethyl Ester: A Mild Route to Mesalazine

Abstract: Photoexcited TiO2 dispersed in a de-aerated acetonitrile/2-propanol (CH3CN/2-PrOH) reaction mixture catalyzes the quick and selective reduction of 5-nitrosalicylic acid methyl ester to the corresponding aniline, an immediat

A convenient method for synthesizing modified 4-nitrophenols

β-Nitroenamine having a formyl group behaves as the synthetic equivalent of unstable nitromalonaldehyde upon treatment with ketones under basic conditions and leads to 2,6-disubstituted 4-nitrophenols. The present method is safer than the conventional one using sodium nitromalonaldehyde and enables the preparation of hitherto unknown nitrophenols.

Benzoxazepinones and their use as squalene synthase inhibitors

There is disclosed a compound represented by the formula [I]: wherein R1 is optionally substituted 1-carboxyethyl group, optionally substituted alkyl-sulfonyl group, optionally substituted (carboxy-cycloalkyl)-alkyl group, -X1-X2-Ar-X3-X4-COOH (wherein X1 and X4 are a bond or alkylene group, X2 and X3 are a bond, -O-, -S-, Ar is divalent aromatic group etc.), R2 is alkyl group optionally substituted with alkanoyloxy group and/or hydroxy group, R3 is alkyl group, and W is halogen atom, etc., or a salt thereof. The compound has the cholesterol lowering activity and the triglyceride lowering activity and is useful for preventing and/or treating hyperlipidemia.