56670-20-3

Basic information

• Product Name: 4-DIMETHYLAMINO-2-NITROBENZALDEHYDE 97
• Synonyms: 4-DIMETHYLAMINO-2-NITROBENZALDEHYDE 97;4-Dimethylamino-2-nitrobenzaldehyde 97%
• CAS NO: 56670-20-3
• Molecular Formula: C₉H₁₀N₂O₃
• Molecular Weight: 194.189
• Product Categories: Aldehydes;C9;Carbonyl Compounds
• Mol File: 56670-20-3.mol

Chemical Properties

• Melting Point: 117 °C (dec.)(lit.)
• Boiling Point: 365.5°C at 760 mmHg
• Flash Point: 174.8°C
• Appearance: /
• Density: 1.286g/cm³
• Vapor Pressure: 1.57E-05mmHg at 25°C
• Refractive Index: 1.632
• Storage Temp.: Inert atmosphere,Room Temperature
• PKA: -0.70±0.22(Predicted)
• CAS DataBase Reference: 4-DIMETHYLAMINO-2-NITROBENZALDEHYDE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 4-DIMETHYLAMINO-2-NITROBENZALDEHYDE 97(56670-20-3)
• EPA Substance Registry System: 4-DIMETHYLAMINO-2-NITROBENZALDEHYDE 97(56670-20-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 56670-20-3(Hazardous Substances Data)

Usage

Uses

Used in Chemical Synthesis:
4-Dimethylamino-2-nitrobenzaldehyde 97 is used as a key intermediate in the synthesis of various substituted 4-(dimethylamino)-6-nitrobenzaldehydes for different applications in the chemical industry. These substituted compounds can be utilized in the development of pharmaceuticals, dyes, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Dimethylamino-2-nitrobenzaldehyde 97 is used as a starting material for the synthesis of various active pharmaceutical ingredients. The substituted 4-(dimethylamino)-6-nitrobenzaldehydes derived from this compound can be further modified to create new drugs with potential therapeutic applications.
Used in Dye Industry:
4-Dimethylamino-2-nitrobenzaldehyde 97 is also used as a precursor in the dye industry for the production of various organic dyes. The substituted 4-(dimethylamino)-6-nitrobenzaldehydes synthesized from this compound can be used to create a wide range of dyes with different color properties, which can be applied in various industries such as textiles, plastics, and printing.
Used in Research and Development:
In the field of research and development, 4-Dimethylamino-2-nitrobenzaldehyde 97 is used as a versatile building block for the synthesis of novel organic compounds with potential applications in various fields. Researchers can explore the chemical properties and reactivity of this compound to develop new synthetic routes and create innovative products.

InChI:InChI=1/C9H10N2O3/c1-10(2)8-4-3-7(6-12)9(5-8)11(13)14/h3-6H,1-2H3

Upstream product

• 619-31-8 N,N-dimethyl-3-nitroaniline 
• 67-64-1 acetone 

Downstream Products

• 109466-82-2 (4-[1,3]Dioxolan-2-yl-3-nitro-phenyl)-dimethyl-amine 
• 56669-96-6 2-amino-4-(N,N-dimethylamino)benzaldehyde 
• 109466-83-3 4-[1,3]Dioxolan-2-yl-N¹,N¹-dimethyl-benzene-1,3-diamine 
• 93836-01-2 Ethyl-α-carbethoxy-4-dimethylamino-2-nitrocinnamate 
• 57470-67-4 2-nitro-4-dimethylaminobenzaldehydephenylhydrazone 
• 296230-77-8 (E) ethyl 3-(4-dimethylamino-2-nitrophenyl)-2-methyl-2-propenate 
• 1391935-02-6 (E)-4-(2,6-Difluorostyryl)-N₁,N₁-dimethylbenzene-1,3-diamine 
• 1391935-05-9 (E)-N-(2-(2,6-difluorostyryl)-5-(dimethylamino)phenyl)-5-(2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide 
• 1391935-01-5 (E)-4-(2,6-Difluorostyryl)-N,N-dimethyl-3-nitroaniline 
• 1374107-30-8 2-(4-fluorophenyl)-7-dimethylaminoquinoline 
• 1610368-34-7 N,N-dimethyl-2-phenyl-2H-indazol-6-amine 
• 1613452-89-3 2,6-bis-(4-dimethylamino-2-nitrobenzylidene)cyclohexanone 
• 1613452-97-3 3,5-bis[4-(dimethylamino)-2-nitrobenzylidene]piperidin-4-one 

Relevant articles and documents

Caged amino acids

The caged amino acid in accordance with the present invention has the structure represented by the following formula 1: where X and Y each represent a halogen atom, an alkyl group, an alkyloxy group, an alkylamino group, or a benzo group; R1represents a hydrogen atom or an alkyl group; R2and R3each represent a hydrogen atom or an alkyl group; A represents an amino acid residue; and M represents a hydrogen atom, an alkali metal, or an alkaline-earth metal.

Production of aminobenzaldehydes

Aminobenzaldehyde compounds and a process for their production by the reaction of an aniline with a formamide in the presence of an acid halide with or without a following reaction with a nitrogen compound. The products are starting materials for the prod