May cause an allergic skin reaction. Chemsrc provides 4-Nitrobenzaldehyde(CAS#:555-16-8) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Guidechem provides 4-Nitrobenzaldehyde chemical database query, including CAS registy number 555-16-8, 4-Nitrobenzaldehyde MSDS (Material Safety Data Sheet), nature, English name, manufacturer, function/use, molecular weight, density, boiling point, melting point, structural formula, etc. It undergoes simultaneous oxidation and reduction with alcoholic potassium hydroxide, giving potassium benzoate and benzyl alcohol. Acute aquatic toxicity. Benzaldehyde is formed by partial oxidation of benzyl alcohol and readily oxidized to benzoic acid and is converted to addition products by hydrocyanic acid or sodium bisulfite. to yellow Powder, Slightly soluble
It is used chiefly in the synthesis of other organic compounds, ranging from pharmaceuticals to plastic additives and benzaldehyde is an important intermediate for the processing of perfume and flavouring compounds and in the preparation of certain aniline dyes. SPECIFIC GRAVITY : 1.496. 209-084-5: FORMULA: ... MELTING POINT : 106 C. BOILING POINT . Two different types of aldehydes (aromatic and aliphatic) can undergo crossing reaction to form fomaldehyde and aromatic alcohols. It is converted to benzoin with alcoholic potassium cyanide, with anhydrous sodium acetate and acetic anhydride, giving cinnamic acid. 4-Nitrobenzaldehyde is an organic aromatic compound containing a nitro group para-substituted to an aldehyde.. Nitrobenzyldiacetate is obtained by the reaction of 4-nitrotoluene and chromium(VI) oxide in acetic anhydride. in water (very soluble in ethanol), Health hazard: 2, Flammability: 0, Physical hazards: 0. White
Causes serious eye irritation. It is also prepared by oxidation of toluene or benzyl chloride or by treating benzal chloride with an alkali, e.g., sodium hydroxide. It boils at 180°C, is soluble in ethanol, but is insoluble in water. The speed of the reaction depends on the substituents in the aromatic ring. Service Tel: +86-571-87759741, Marketing Tel: +86-571-89739798 skype, Copyright©2010-2020 Guidechem 浙B2-20090288-37. Harmful to aquatic life. GHS (Globally Harmonised System) Classification: Skin irritation. Aromatic aldehydes such as benzaldehyde and formaldehyde may undergo disproportionation in concentrated alkali (Cannizaro's reaction); one molecule of the aldehyde is reduced to the corresponding alcohol and another molecule is simultaneously oxidized to the salt of a carboxylic acid. Product # Description 130176: 4-Nitrobenzaldehyde, 98%, 72800: 4-Nitrobenzaldehyde, for spectrophotometric det. Find chemicals information 4-Nitrobenzaldehyde at guidechem, professional and easy to use.