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(2E,6Z)-2-[(DIMETHYLAMINO)METHYLENE]-6-[(2E)-2-(3-ETHYL-1,3-BENZOTHIAZOL-2(3H)-YLIDENE)ETHYLIDENE]CYCLOHEXANONE is a complex organic compound characterized by a cyclohexanone ring and two distinct functional groups: dimethylamino and benzothiazol-3-ylidene. The dimethylamino group forms a methylene bridge, while the benzothiazol-3-ylidene group contributes to the formation of an ethylidene bridge. This unique structure and the presence of these functional groups make it a versatile molecule in the field of organic chemistry.

88340-50-5

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88340-50-5 Usage

Uses

Used in Organic Synthesis:
(2E,6Z)-2-[(DIMETHYLAMINO)METHYLENE]-6-[(2E)-2-(3-ETHYL-1,3-BENZOTHIAZOL-2(3H)-YLIDENE)ETHYLIDENE]CYCLOHEXANONE serves as a key intermediate in organic synthesis, allowing for the creation of a variety of complex organic molecules. Its unique structure and functional groups facilitate multiple reaction pathways, making it a valuable component in the synthesis of new compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (2E,6Z)-2-[(DIMETHYLAMINO)METHYLENE]-6-[(2E)-2-(3-ETHYL-1,3-BENZOTHIAZOL-2(3H)-YLIDENE)ETHYLIDENE]CYCLOHEXANONE acts as a building block for the development of new drugs. Its specific structural features and functional groups can be leveraged to design and synthesize pharmaceuticals with targeted therapeutic effects.
Used in Dye Manufacturing:
(2E,6Z)-2-[(DIMETHYLAMINO)METHYLENE]-6-[(2E)-2-(3-ETHYL-1,3-BENZOTHIAZOL-2(3H)-YLIDENE)ETHYLIDENE]CYCLOHEXANONE is also utilized in the production of dyes due to its ability to form stable chromophores. Its incorporation into dye molecules can lead to the development of dyes with specific color characteristics and improved properties, such as stability and solubility.
Used in Other Organic Compounds Production:
Beyond its applications in organic synthesis, pharmaceuticals, and dyes, (2E,6Z)-2-[(DIMETHYLAMINO)METHYLENE]-6-[(2E)-2-(3-ETHYL-1,3-BENZOTHIAZOL-2(3H)-YLIDENE)ETHYLIDENE]CYCLOHEXANONE is employed as a component in the synthesis of other organic compounds. Its versatility and unique structural elements make it suitable for a wide range of applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 88340-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,4 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88340-50:
(7*8)+(6*8)+(5*3)+(4*4)+(3*0)+(2*5)+(1*0)=145
145 % 10 = 5
So 88340-50-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H24N2OS/c1-4-22-17-10-5-6-11-18(17)24-19(22)13-12-15-8-7-9-16(20(15)23)14-21(2)3/h5-6,10-14H,4,7-9H2,1-3H3/b15-12-,16-14+,19-13+

88340-50-5SDS

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 2-(dimethylaminomethylidene)-6-[2-(3-ethyl-1,3-benzothiazol-2-ylidene)ethylidene]cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names Cyclohexanone,2-[(dimethylamino)methylene]-6-[2-(3-ethyl-2(3H)-benzothiazolylidene)ethylidene]

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:88340-50-5 SDS

88340-50-5Downstream Products

88340-50-5Relevant academic research and scientific papers

POLYMETHINE DYES WITH HYDROCARBON BRIDGES. ENAMINO KETONES IN THE CHEMISTRY OF CYANINE DYES

Slominskii, Yu. L,Radchenko, I. D.,Popov, S. V.,Tolmachev, A. I.

, p. 1854 - 1860 (2007/10/02)

In the presence of bases alicyclic enamino ketones can react both with methyl- and with β-dialkylaminovinyl-substituted quaternary salts of nitrogen heterocycles.The reaction leads to the formation of merocyanines in which part of the chromophore extends

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