30095-98-8

Basic information

• Product Name: METHYL (2-NITRO-PHENYL)-ACETATE
• Synonyms: METHYL 2-(2-NITROPHENYL)ACETATE;METHYL (2-NITRO-PHENYL)-ACETATE;(2-Nitrophenyl)acetic acid, methyl ester;2-(2-Nitrophenyl)acetic acid methyl;2-Nitrobenzeneacetic acid methyl;Benzeneaceticacid, 2-nitro-, Methyl ester;METHYL2-(2-NITHROPHENYL)-ACETATE;o-Nitrophenylacetic acid methyl ester
• CAS NO: 30095-98-8
• Molecular Formula: C₉H₉NO₄
• Molecular Weight: 195.17
• Mol File: 30095-98-8.mol
• Article Data: 65

Chemical Properties

• Boiling Point: 283.4 °C at 760 mmHg
• Flash Point: 126.5 °C
• Appearance: /
• Density: 1.266 g/cm³
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: METHYL (2-NITRO-PHENYL)-ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL (2-NITRO-PHENYL)-ACETATE(30095-98-8)
• EPA Substance Registry System: METHYL (2-NITRO-PHENYL)-ACETATE(30095-98-8)

Safety Data

• Hazardous Substances Data: 30095-98-8(Hazardous Substances Data)

Usage

General Description

Methyl (2-nitro-phenyl)-acetate is an organic compound with the chemical formula C9H9NO4. It is a yellow crystalline solid that is commonly used as a fragrance ingredient in perfumes and colognes. METHYL (2-NITRO-PHENYL)-ACETATE is known for its fruity and floral odor, and it is often used to add a sweet, refreshing scent to various consumer products. Methyl (2-nitro-phenyl)-acetate is also used in the synthesis of pharmaceuticals and other organic compounds due to its versatile chemical properties. However, it is important to handle this chemical with care, as it can be harmful if ingested or inhaled, and it may cause irritation to the skin and eyes.

Upstream product

• 101-41-7 benzeneacetic acid methyl ester 
• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 3958-60-9 2-nitrophenylmethyl bromide 
• 1360789-03-2 2-(2-nitrophenyl)-1-(2,2,6,6-tetramethylpiperidin-1-yl)ethanone 
• 274676-13-0 methyl (+/-)-2-(2-nitrophenyl)-4-pentenoate 
• 22751-23-1 (2-nitrophenyl)acetyl chloride 
• 1493-27-2 ortho-nitrofluorobenzene 
• 365-33-3 2-nitrobenzenediazonium tetrafluoroborate 
• 107-13-1 acrylonitrile 
• 3740-52-1 2-(2-nitrophenyl)acetic acid 
• 1336-21-6 ammonium hydroxide 
• 26465-37-2 dimethyl 2-(2-nitrophenyl)malonate 
• 74-88-4 methyl iodide 

Downstream Products

• 59-48-3 2-oxoindole 
• 35613-44-6 2-aminophenylacetic acid methyl ester 
• 136764-88-0 2-Methyl-2-(2-nitro-phenyl)-butyric acid methyl ester 
• 57486-45-0 2-Nitrophenylacetylguanidin 
• 21859-90-5 (1,1-D⁽²⁾)-2-(2-Nitro-phenyl)-aethanol 
• 251982-40-8 (Z)-methyl (2-nitrophenyl)(phenylimino)acetate N-oxide 
• 18108-55-9 1,3-dihydro-1-hydroxyindole-2-one 
• 274676-14-1 methyl (+/-)-4-methyl-2-(2-nitrophenyl)-4-pentenoate 
• 340269-68-3 methyl (+/-)-4-tert-butyl-2-(2-nitrophenyl)-4-pentenoate 
• 274676-13-0 methyl (+/-)-2-(2-nitrophenyl)-4-pentenoate 
• 494836-60-1 methyl α-(2-nitrophenyl)acrylate 
• 777864-66-1 methyl 2-(2-nitrophenyl)pent-4-ynoate 
• 870456-18-1 (E)-methyl 2-(2-nitrophenyl)but-2-enoate 
• 924621-31-8 methyl 7-methyl-4-methylene-2-(2-nitrophenyl)oct-7-enoate 

Relevant articles and documents

Dihalide impurity in ziprasidone hydrochloride intermediate and preparation method of dihalide impurity

The invention provides a dihalide impurity in a ziprasidone hydrochloride intermediate. The dihalide impurity has a structure shown as a formula 1. On the basis that the ziprasidone hydrochloride intermediate can bring in the dechlorination impurity or the preparation process contains the dechlorination step, the dechlorination impurity with a specific structure is obtained, and the preparation steps of the corresponding impurity are provided, so a corresponding technical support is provided for preparation of ziprasidone hydrochloride. The synthesis method provided by the invention has the advantages of simple process, strong controllability and mild conditions, can be used for quality standard establishment and quality control links of ziprasidone hydrochloride process research and development, production and the like, and provides technical support for ziprasidone hydrochloride medication safety. The method can be used for quality research such as qualitative and quantitative analysis of impurities in ziprasidone hydrochloride synthesis, so that the quality of ziprasidone hydrochloride can be improved, and important guiding significance is provided for reducing the medication risk of ziprasidone hydrochloride.

SUBSTITUTED IMIDAZOLECARBOXAMIDE AS BRUTON'S TYROSINE KINASE INHIBITORS

The disclosure relates to a series of substituted imidazolecarboxamide compounds of formula I as BTK (Bruton's Tyrosine Kinase) inhibitors, and the methods of using the same for the treatment of autoimmune disease, inflammatory disease, cancer and potenti

Synthesis process of diclofenac sodium

The invention provides a synthesis process of diclofenac sodium, which is obtained by acylation reaction of o-aminobenzene acetate with 2 and 6 - dichlorophenoxy acetic acid respectively and acylation with chlorobenzoyl chloride followed by nucleophilic substitution with 2, 6 - dichlorophenol or 2 and 6 -dichlorophenol. Is hydrolyzed to give sodium diclofenac sodium. The synthesis process is simplified, the reaction condition is mild, and the yield and industrial popularization and application are facilitated.