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4-nitro-N-(9H-xanthen-9-yl)benzamide is a complex organic compound with the molecular formula C20H14N4O4. It is characterized by the presence of a nitro group (-NO2) attached to a benzene ring, which is also connected to a benzamide group (-CO-NH2). The xanthene moiety, which is a tricyclic aromatic system, is fused to the benzene ring through a methylene bridge. 4-nitro-N-(9H-xanthen-9-yl)benzamide is known for its potential applications in the field of chemistry, particularly in the synthesis of dyes and fluorescent markers. Its structure and properties make it a subject of interest for researchers exploring the behavior of complex molecules and their interactions in various chemical and biological systems.

6326-02-9

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6326-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6326-02-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6326-02:
(6*6)+(5*3)+(4*2)+(3*6)+(2*0)+(1*2)=79
79 % 10 = 9
So 6326-02-9 is a valid CAS Registry Number.

6326-02-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitro-benzoic acid xanthen-9-ylamide

1.2 Other means of identification

Product number -
Other names Dimethyl-ethyl-carbinyl-p-nitrobenzoat

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:6326-02-9 SDS

6326-02-9Downstream Products

6326-02-9Relevant academic research and scientific papers

RuV-Acylimido Intermediate in [RuIV(Por)Cl2]-Catalyzed C–N Bond Formation: Spectroscopic Characterization, Reactivity, and Catalytic Reactions

Che, Chi-Ming,Hong, Dan-Yan,Huang, Jie-Sheng,Law, Siu-Man,Liu, Yungen,Lo, Vanessa Kar-Yan,Toy, Patrick H.,Wu, Liangliang

supporting information, p. 18619 - 18629 (2021/06/09)

Metal-catalyzed C?N bond formation reactions via acylnitrene transfer have recently attracted much attention, but direct detection of the proposed acylnitrenoid/acylimido M(NCOR) (R=aryl or alkyl) species in these reactions poses a formidable challenge. H

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