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5-acetyl-2-phenylamino-3-nitrothiophene is a complex organic chemical compound with the molecular formula C12H9N2O3S. It is characterized by the presence of a thiophene ring, which is a five-membered aromatic ring containing one sulfur atom. The molecule features a nitro group (NO2) at the 3-position, an acetyl group (COCH3) at the 5-position, and a phenylamino group (C6H5NH) at the 2-position. 5-acetyl-2-phenylamino-3-nitrothiophene is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is an important intermediate in the preparation of certain dyes and pigments, as well as in the development of new materials with specific optical and electronic properties. The compound's synthesis often involves multi-step processes, and its handling requires careful consideration of its reactivity and potential hazards.

1087-13-4

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1087-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1087-13-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1087-13:
(6*1)+(5*0)+(4*8)+(3*7)+(2*1)+(1*3)=64
64 % 10 = 4
So 1087-13-4 is a valid CAS Registry Number.

1087-13-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-acetyl-2-phenylamino-3-nitrothiophene

1.2 Other means of identification

Product number -
Other names 2-Anilino-5-acetyl-3-nitrothiophen

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1087-13-4 SDS

1087-13-4Downstream Products

1087-13-4Relevant academic research and scientific papers

Aromatic Nucleophilic Substitution Reactions of Some 3-Nitro-2-p-nitrophenoxy-5-X-thiophenes with Substituted Anilines in Methanol

Consiglio, Giovanni,Frenna, Vincenzo,Guernelli, Susanna,Macaluso, Gabriella,Spinelli, Domenico

, p. 770 - 781 (2007/10/03)

The kinetic constants for the reaction of some 3-nitro-2-p-nitrophenoxy-5-X-thiophenes (X = H, Br, CONH2, CO2Me, Ac, SO2Me, CN,NO2) with some substituted anilines YC6H4NH2 (Y = p-OMe, p-Me, H, n-Cl, p-Cl) have been measured at various temperatures and a s

Aromatic Nucleophilic Substitution Reactions of Some 2-L-3-Nitro-5-X-thiophenes with Piperidine and Aniline in Methanol. Substituent Constants for the Thiophene System

Consiglio, Giovanni,Frenna, Vincenzo,Arnone, Caterina,Mezzina, Elisabetta,Spinelli, Domenico

, p. 2187 - 2190 (2007/10/02)

The rate constants for the reactions of some 2-L-3-nitro-5-X-thiophenes 1-4 with aniline and of compounds (4) with piperidine in methanol have been measured at various temperatures.By using the data obtained in this work as well as previously available data sets, a series of optimized 'thiophene' ?τ values has been calculated.The susceptibility constants ρ(L) of the various sets have been analysed in the framework of the reactivity-selectivity principle.

NUCLEOPHILIC SUBSTITUTION REACTIONS ON CHLORINATED THIOPHENE DERIVATIVES AS BASIS FOR THE SYNTHESIS OF THIENOANELLATED O,N- AND S,N-HETEROCYCLES

Puschmann, Isolde,Erker, Thomas

, p. 1323 - 1332 (2007/10/02)

The reactivity of 5-acetyl-2-chloro-3-nitrothiophene with amines, alcohols, thiols and bifunctional compounds, as well as reactions of methyl 5-chloro-4-nitro-2-thiophenecarboxylate with various hydrazides are described.These substitution reactions provid

Linear Free Energy Relationships in the Thiophen Series. Part 2. The Kinetics of the Reactions of Some 2-Bromo-3-nitro-5-X-thiophens with Substituted Anilines in Methanol

Consiglio, Giovanni,Arnone, Caterina,Spinelli, Domenico,Noto, Renato,Frenna, Vincenzo

, p. 388 - 392 (2007/10/02)

The rate constants for the reactions of 2-bromo-3-nitro-5-X-thiophens (X=H, Br, CONH2, CO2Me, Ac, SO2Me, CN, or NO2) with some substituted anilines YC6H4NH2 (Y=p-OMe, p-Me, H, m-Cl, or p-CO2Me) have been measured in methanol at various temperatures.The se

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