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N-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-N-phenylacetamide is a complex organic compound with the molecular formula C16H11ClNO3. It is characterized by a naphthalene ring system, which is a fused ring structure consisting of two benzene rings. The compound features a 3-chloro substituent, indicating the presence of a chlorine atom at the 3-position of the naphthalene. Additionally, it has a 1,4-dioxo group, which refers to two oxygen atoms double-bonded to carbon atoms at the 1 and 4 positions, effectively forming two carbonyl groups. The compound is further described by a 1,4-dihydronaphthalen-2-yl group, suggesting that the naphthalene ring is partially reduced, and an acetamide group is attached to the 2-position of the naphthalene. The acetamide group consists of an amide linkage between an acetic acid molecule and an amine group, with the phenyl group (a benzene ring) attached to the nitrogen atom of the amide. N-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-N-phenylacetamide is likely to be used in chemical research or as an intermediate in the synthesis of pharmaceuticals or other organic compounds due to its unique structure and functional groups.

4497-73-8

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4497-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4497-73-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,9 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4497-73:
(6*4)+(5*4)+(4*9)+(3*7)+(2*7)+(1*3)=118
118 % 10 = 8
So 4497-73-8 is a valid CAS Registry Number.

4497-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chlor-2-acetamidofluoren

1.2 Other means of identification

Product number -
Other names 3-Chloro-2-acetylaminofluorene

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

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More Details:4497-73-8 SDS

4497-73-8Relevant academic research and scientific papers

A simple synthesis of 3,4-dihydrobenzo[f]quinoxalin-6(2H)-one derivatives substituted in the ring B

Castro-Castillo, Vicente,Suárez-Rozas, Cristian,Simpson, Sebastián,Barriga-González, Andrés

, p. 553 - 559 (2017/08/30)

[Figure not available: see fulltext.] We followed a simple, inexpensive, and efficient route to synthesize a series of 3,4-dihydrobenzo[f]quinoxalin-6(2H)-one derivatives substituted in the ring B, with the expectation that this scaffold might exhibit antineoplastic activity. 5-Chlorobenzo[f]quinoxalin-6-ylacetate and 4-benzylbenzo[f]quinoxalin-6(4H)-one were obtained for the first time.

Angular Heterocycles. A Convenient Synthesis of 6-N-(Acetylanilino)-5H-benzophenothiazin-5-one, 6-N-(Acetylanilino)-5H-benzophenoxazin-5-ones and Their Derivatives

Agarwal, N. L.,Ghosh, S.,Tripathi, A. K.,Atal, C. K.

, p. 509 - 512 (2007/10/02)

The reaction of 2-N-(acetylanilino)-3-chloro-1,4-naphthoquinone (2) with bifunctional aromatic amines afforded angular heterocycles 6 and 7.Reductive acetylation of 7 provided O-acyl 9 and O,N-diacyl 10 derivatives depending upon the reaction conditions.T

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