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1-[4-(Methylamino)-3-nitrophenyl]ethan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18076-17-0

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18076-17-0 Usage

Appearance

Yellow crystalline powder

Usage

Reagent in organic synthesis

Structural features

Nitro group (-NO2) attached to a phenyl ring
Methylamino group (-NH-CH3) attached to a phenyl ring
Ethanone moiety (-CO-CH3)

Industry applications

Pharmaceutical industry for drug preparation

Synthesis utility

Building block for complex organic molecules

Research and development

Study of organic reactions and development of new chemical processes

Check Digit Verification of cas no

The CAS Registry Mumber 18076-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,7 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18076-17:
(7*1)+(6*8)+(5*0)+(4*7)+(3*6)+(2*1)+(1*7)=110
110 % 10 = 0
So 18076-17-0 is a valid CAS Registry Number.

18076-17-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-(Methylamino)-3-nitrophenyl]ethanone

1.2 Other means of identification

Product number -
Other names 4-Methylamino-3-nitro-acetophenon

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:18076-17-0 SDS

18076-17-0Relevant academic research and scientific papers

Substituted Fused Imidazole Derivatives, Pharmaceutical Compositions, and Methods of Use Thereof

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Page/Page column 146, (2011/09/14)

Substituted fused imidazole derivatives, methods of their preparation, pharmaceutical compositions comprising a substituted fused imidazole derivative, and methods of use in treating inflammation are provided. The substituted fused imidazole derivatives may control the activity or the amount or both the activity and the amount of heme-oxygenase.

VIRAL POLYMERASE INHIBITORS

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Page/Page column 74, (2008/06/13)

An enantiomer, diastereoisomer or tautomer of a compound, represented by formula (I): wherein either A or B is nitrogen and the other B or A is C, and the radicals R1, R2, R3, R4, R5, R6, R7, R8, R9, and R10 are as defined herein, or a salt or ester thereof as viral polymerase inhibitors. The compound is used as an inhibitor of RNA dependent RNA polymerases, particularly those viral polymerases within the Flaviviridae family, more particularly to HCV polymerase.

(1H-imidazol-1-ylmethyl) substituted benzimidazole derivatives and use thereof in treating androgen dependent disorders

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, (2008/06/13)

Novel (1H-imidazol-1-ylmethyl) substituted benzimidazole derivatives, compositions containing the same, and methods of treating androgen dependent disorders in mammals.

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