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4497-58-9

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4497-58-9 Usage

Description

1,2,3,4-Tetrahydro-2,2,4-trimethylquinoline is an organic compound with a quinoline structure, featuring a tetrahydro group and three methyl groups attached to specific positions on the molecule. 1,2,3,4-Tetrahydro-2,2,4-trimethylquinoline is known for its unique chemical properties and potential applications in various industries.

Uses

Used in Solar Cell Industry:
1,2,3,4-Tetrahydro-2,2,4-trimethylquinoline is used as a reagent for the synthesis of tetrahydroquinoline sensitizers. These sensitizers are crucial components in the development of dye-sensitized solar cells, which are a type of photovoltaic cell that relies on the absorption of light by organic pigments to generate electricity.
Used in Photoantimicrobial Applications:
1,2,3,4-Tetrahydro-2,2,4-trimethylquinoline is also utilized as a reagent in the preparation of tetraand pentacyclic derivatives of phenothiazinium photosensitizers. These photosensitizers are employed as photoantimicrobial agents, which are used to combat and inhibit the growth of microorganisms, such as bacteria and fungi, through the use of light-activated chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 4497-58-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,9 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4497-58:
(6*4)+(5*4)+(4*9)+(3*7)+(2*5)+(1*8)=119
119 % 10 = 9
So 4497-58-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H17N/c1-9-8-12(2,3)13-11-7-5-4-6-10(9)11/h4-7,9,13H,8H2,1-3H3

4497-58-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4-trimethyl-3,4-dihydro-1H-quinoline

1.2 Other means of identification

Product number -
Other names 2,4,4-trimethyl-1,2,3,4-tetrahydroquinoline

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:4497-58-9 SDS

4497-58-9Relevant articles and documents

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Brown,Meth-Cohn

, p. 3631,3633 (1971)

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Engineering of highly efficient tetrahydroquinoline sensitizers for dye-sensitized solar cells

Hao, Yan,Yang, Xichuan,Cong, Jiayan,Hagfeldt, Anders,Sun, Licheng

, p. 552 - 558 (2012/01/06)

Four novel tetrahydroquinoline dyes by inserting isophorone and/or thiophene moieties as π bridge between the electron donating unit of substituted tetrahydroquinoline and the electron withdrawing unit of cyano carboxylic acid have been synthesized and successfully applied to dye-sensitized solar cells. Among them, DSCs sensitized by HYTIC, which shows the simplest molecular structure, exhibit improved efficiency of 7.0%. This by now is the highest efficiency for the reported tetrahydroquinoline sensitizers and comparable to the performance of N719-sensitized solar cells under the conditions employed here.

BENZAMIDIC COMPOUNDS HAVING FUNGICIDAL ACTIVITY AND RELATIVE USE

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Page/Page column 15, (2010/12/01)

The present invention relates to benzamidic compounds having general formula (I): wherein: Rx represents a halogen atom or a methyl group possibly substituted by fluorine atoms; R1, R2, R3, independently from each other, represent a C1- C3 alkyl group; R4 represents a hydrogen atom or a C1-C3 alkyl group; Ry represents a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alcoxy group, a C1-C4 haloalcoxy group; n represents an integer ranging of from 0 to 3. The present invention also relates to the use of the above benzamidic compounds for the control of fungi, bacteria and phytopathogenic viruses of agricultural crops.

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