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9H-Carbazole,9,9'-methylenebis-, also known as 4,5-Methylenedi-9H-carbazole, is an organic compound with the chemical formula C20H14N2. It is a white crystalline solid that is insoluble in water but soluble in organic solvents such as ethanol and acetone. 9H-Carbazole,9,9'-methylenebis- is characterized by its unique structure, featuring two carbazole rings connected by a methylene bridge. It is primarily used as a precursor in the synthesis of various dyes, pigments, and pharmaceuticals due to its ability to form stable and vibrant colors. Additionally, it has been studied for its potential applications in the field of organic electronics, such as in the development of organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs), where its electronic properties and stability are of interest.

6510-63-0

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6510-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6510-63-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,1 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6510-63:
(6*6)+(5*5)+(4*1)+(3*0)+(2*6)+(1*3)=80
80 % 10 = 0
So 6510-63-0 is a valid CAS Registry Number.

6510-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Di-carbazol-9-yl-methan

1.2 Other means of identification

Product number -
Other names Dicarbamoylmethyl-carbamidsaeure-aethylester

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:6510-63-0 SDS

6510-63-0Downstream Products

6510-63-0Relevant academic research and scientific papers

PHOTOCHEMICAL REACTION OF CARBAZOLE AND SOME DERIVATIVES IN DICHLOROMETHANE

Balsells, R. Erra,Frasca, A. R.

, p. 5363 - 5366 (2007/10/02)

By irradiation of carbazole and some derivatives in CH2Cl2 soln two different reaction pathways were observed depending on the substitution of the heterocyclic compound.

REACTION OF 9-(HYDROXYMETHYL)CARBAZOLES WITH PHENOLS

Tolmacheva, V. Ya.,Zherebtsov, I. P.,Lopatinskii, V. P.,Shardakova, N. I.

, p. 138 - 143 (2007/10/02)

The reaction of 9-(hydroxymethyl)carbazole with unsubstituted phenols and phenols substituted in the ring with electron-donating groups in the absence of catalysts leads to the formation of the corresponding 9-(2-hydroxybenzyl)carbazoles.In an acidic medium the reaction of phenol with 9-(hydroxymethyl)carbazole leads to 3-(2-hydroxybenzyl)carbazole.In the absence of catalysts the reaction takes place thropugh an intermediate chelate, and in the presence of acids the aminomethylating agent is a carbenium-immonium ion.

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