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115704-83-1

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115704-83-1 Usage

Description

Tetramethyljulolidine, also known as 1,1,7,7-Tetramethyl-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-8-ol, is an organic compound that serves as a valuable reactant in the synthesis of various complex organic molecules. It is characterized by its unique molecular structure, which includes nitrogen-containing fused rings, making it a versatile building block in organic chemistry.

Uses

Used in Organic Synthesis:
Tetramethyljulolidine is used as a reactant for the preparation of aminobenzopyranoxanthenes with nitrogen-containing fused rings. Its unique molecular structure allows for the creation of complex organic molecules that can be utilized in various applications, such as pharmaceuticals, dyes, and advanced materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Tetramethyljulolidine is used as a key intermediate in the synthesis of various drug molecules. Its nitrogen-containing fused rings provide a structural framework that can be further modified to develop new drugs with specific therapeutic properties.
Used in Dye Industry:
Tetramethyljulolidine can be used as a building block for the development of novel dyes with unique color properties. Its nitrogen-containing fused rings can be modified to create dyes with improved stability and color intensity.
Used in Advanced Materials:
The unique molecular structure of Tetramethyljulolidine also makes it a promising candidate for the development of advanced materials with specific properties, such as optoelectronic materials, sensors, and catalysts. Its nitrogen-containing fused rings can be tailored to achieve desired characteristics for these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 115704-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,7,0 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115704-83:
(8*1)+(7*1)+(6*5)+(5*7)+(4*0)+(3*4)+(2*8)+(1*3)=111
111 % 10 = 1
So 115704-83-1 is a valid CAS Registry Number.

115704-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,7,7-Tetramethyl-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-8-ol

1.2 Other means of identification

Product number -
Other names 1,1,7,7-tetramethyl-8-hydroxyjulolidine

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:115704-83-1 SDS

115704-83-1Relevant articles and documents

Synthesis of unsymmetrical 4-oxo-2-vinyl-4H-chromene-3-carbonitrile dyes via Knoevenagel reaction

Levchenko,Chudov,Zinoviev,Lyssenko,Demin,Poroshin,Shmelin,Grebennikov

, p. 2788 - 2792 (2018/06/08)

New 4-oxo-2-vinyl-4H-chromene-3-carbonitrile derivatives have been synthesized by the Knoevenagel reaction of 2-methyl-4-oxo-4H-chromene-3-carbonitrile with aromatic and heteroaromatic aldehydes. Spectral properties of the obtained compounds have been studied.

3,6-DISUBSTITUTED XANTHYLIUM SALTS

-

Page/Page column 87, (2010/07/02)

This invention pertains generally to processes, uses, methods and materials utilising particular xanthylium compounds, including compounds of formula (I) and (II), as further defined herein. These compounds are useful as drugs, for example, in the treatment of tauopathies, such as Alzheimer's disease.

Synthesis of 5- and 6-carboxy-x-rhodamines

Uddin, Md Jashim,Marnett, Lawrence J.

supporting information; experimental part, p. 4799 - 4801 (2009/05/31)

(Equation Presented) An efficient route is reported to 5- and 6-carboxy-X-rhodamines (compounds 1 and 2) that contain multiple n-propylene or y,y-dimethylpropylene groups bridging terminal nitrogen atoms and the central xanthene core. Gram quantities of these dyes are synthesized from inexpensive starting materials. The isolated products are activated by selective transformation of the carboxylic acid group into N-hydroxysuccinimidyl esters in situ and then conjugated with an amino group of a molecule of interest.

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