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18992-68-2

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18992-68-2 Usage

General Description

1,3-Dimethyl-9H-carbazole is an organic compound that belongs to the carbazole family. It consists of a carbazole core with two methyl groups attached at the 1 and 3 positions. This chemical is commonly used as a building block in organic synthesis and can also be found in some dyes and pigments. It is known for its high thermal stability and ability to form stable complexes with metal ions. Additionally, 1,3-Dimethyl-9H-carbazole has potential applications in the field of organic electronics and optoelectronic devices due to its relatively high electron affinity and good charge transport properties.

Check Digit Verification of cas no

The CAS Registry Mumber 18992-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,9 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18992-68:
(7*1)+(6*8)+(5*9)+(4*9)+(3*2)+(2*6)+(1*8)=162
162 % 10 = 2
So 18992-68-2 is a valid CAS Registry Number.

18992-68-2SDS

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 1,3-Dimethyl-9H-carbazole

1.2 Other means of identification

Product number -
Other names 1,3-dimethyl-carbazole

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:18992-68-2 SDS

18992-68-2Downstream Products

18992-68-2Relevant articles and documents

The Mechanism of the Quinamine Rearrangements

Boduszek, Bogdan,Shine, Henry J.

, p. 3247 - 3252 (2007/10/02)

Acid-catalyzed rearrangement of 6-bromo-2,4-dimethyl-4(phenylamino)cyclohexa-1,4-dienone (1, a quinamine) in aqueous methanol gives, from a so-called quinamine rearrangement, 4'-amino-6-bromo-2,4-dimethyldiphenyl ether (2) and a number of byproducts.The r

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