6970-77-0

Basic information

• Product Name: N-(4,5-DIMETHYL-2-NITRO-PHENYL)-ACETAMIDE
• Synonyms: 4',5'-Dimethyl-2'-nitroacetanilide
• CAS NO: 6970-77-0
• Molecular Formula: C₁₀H₁₂N₂O₃
• Molecular Weight: 208.2187
• Mol File: 6970-77-0.mol
• Article Data: 8

Chemical Properties

• Melting Point: 108 °C(Solv: ethanol (64-17-5))
• Boiling Point: 407.5 °C at 760 mmHg
• Flash Point: 200.2 °C
• Appearance: /
• Density: 1.247g/cm³
• Vapor Pressure: 7.52E-07mmHg at 25°C
• Refractive Index: 1.595
• PKA: 13.84±0.70(Predicted)
• CAS DataBase Reference: N-(4,5-DIMETHYL-2-NITRO-PHENYL)-ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4,5-DIMETHYL-2-NITRO-PHENYL)-ACETAMIDE(6970-77-0)
• EPA Substance Registry System: N-(4,5-DIMETHYL-2-NITRO-PHENYL)-ACETAMIDE(6970-77-0)

Safety Data

• Hazardous Substances Data: 6970-77-0(Hazardous Substances Data)

Usage

General Description

N-(4,5-DIMETHYL-2-NITRO-PHENYL)-ACETAMIDE is a chemical compound with the molecular formula C11H13N3O3. It is a yellow crystalline solid commonly used as an intermediate in the synthesis of various pharmaceutical and agrochemical compounds. This chemical is also known for its use in the production of organic pigments. N-(4,5-DIMETHYL-2-NITRO-PHENYL)-ACETAMIDE is considered to be moderately toxic if ingested or inhaled, and it may cause irritation to the skin and eyes. It is important to handle this chemical with care and adhere to safety guidelines when working with it.

InChI:InChI=1/C10H12N2O3/c1-6-4-9(11-8(3)13)10(12(14)15)5-7(6)2/h4-5H,1-3H3,(H,11,13)

Upstream product

• 6972-71-0 4,5-dimethyl-2-nitrobenzenamine 
• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 
• 619-04-5 3,4-dimethylbenzoic acid 
• 95-64-7 4-amino-o-xylene 
• 7697-37-2 nitric acid 
• 2198-54-1 N-(3,4-dimethylphenyl)acetamide 

Downstream Products

• 6972-71-0 4,5-dimethyl-2-nitrobenzenamine 
• 117044-02-7 acetic acid-(2-amino-4,5-dimethyl-anilide) 
• 89939-49-1 4-amino-5-nitrophthalic acid 
• 52412-57-4 4,5-diaminophthalic acid dimethyl ester 
• 22364-40-5 5-Nitro-4-acetamino-2-methyl-benzylalkohol 
• 22364-41-6 5-Nitro-4-amino-2-methyl-benzylalkohol 
• 22474-47-1 (2-methyl-5-nitro-7-phenyl)methanol 
• 859491-93-3 4,5-dimethyl-2-nitro-phenyl thiocyanate 
• 401936-05-8 bis-(4,5-dimethyl-2-nitro-phenyl)-disulfide 
• 70740-21-5 1-acetyl-5,6-dimethylbenzotriazole 
• 5683-41-0 2,5,6-trimethyl-benzothiazole 
• 68527-69-5 5,6-dimethyl-[8]quinolylamine 
• 3171-45-7 4,5-dimethyl-1,2-phenylenediamine 
• 1027598-42-0 1-Azido-4,5-dimethyl-2-nitro-benzene 

Relevant articles and documents

MACROCYCLIC COMPOUNDS

The present invention relates to macrocyclic compounds which are capable of selective binding to a target saccharide (e.g. glucose), making them particularly well suited for use in saccharide sensing applications. The present invention also relates to processes for the preparation of said compounds, to compositions and devices comprising them, and to their use in the detection of a target saccharide.

SalenZn-bridged D-π-A dyes for dye-sensitized solar cells

A series of SalenZn based dyes with triphenylamine derivatives as the donor, benzoic acid as the acceptor, and coplanar Salen complexes as the spacer have been designed and synthesized for dye-sensitized solar cells. The absorption, electrochemical, and photovoltaic properties for all sensitizers have been systematically investigated. When the tail length of the alkyl substituents is increased from C-0 to C-8 on the donor part, the efficiency of its DSSC augments evidently. It is found that the incorporation of bis-carboxyl groups instead of the single carboxyl group as anchoring groups induces a remarkable enhancement of the electron injection efficiency from the excited dyes to the TiO2 semiconductor and generates higher electron density and voltage. Copyright

Development of a fluorescent indicator for nitric oxide based on the fluorescein chromophore

Endogenous nitric oxide (NO) appears to modulate many physiological and pathophysiological processes. In order to obtain direct evidence for NO functions in vivo, we have developed 4,5-diaminofluorescein (DAF-2) as a novel fluorescent indicator for NO. Gr