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(4Z)-4-(1,3-benzothiazol-2(3H)-ylidene)-2-ethoxycyclohexa-2,5-dien-1-one is a heterocyclic organic compound with the molecular formula C18H17NO2S. It features a benzothiazole ring and exhibits a yellow color. (4Z)-4-(1,3-benzothiazol-2(3H)-ylidene)-2-ethoxycyclohexa-2,5-dien-1-one is frequently utilized in organic synthesis and medicinal chemistry due to its unique structure and reactivity.

6265-95-8

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6265-95-8 Usage

Uses

Used in Pharmaceutical Industry:
(4Z)-4-(1,3-benzothiazol-2(3H)-ylidene)-2-ethoxycyclohexa-2,5-dien-1-one is used as a key intermediate in the synthesis of various pharmaceuticals for its potential biological activities and structural features that can be exploited to develop new drugs.
Used in Agrochemical Industry:
(4Z)-4-(1,3-benzothiazol-2(3H)-ylidene)-2-ethoxycyclohexa-2,5-dien-1-one is also utilized as a building block in the creation of agrochemicals, where its unique structure can contribute to the development of novel pesticides or other agricultural products.
Used in Material Science:
(4Z)-4-(1,3-benzothiazol-2(3H)-ylidene)-2-ethoxycyclohexa-2,5-dien-1-one has potential applications in the development of new materials due to its structural characteristics and reactivity, which can be harnessed to create innovative materials with specific properties.
Used in Chemical Reactions:
Due to its unique structure and reactivity, (4Z)-4-(1,3-benzothiazol-2(3H)-ylidene)-2-ethoxycyclohexa-2,5-dien-1-one may also find use in the development of new chemical reactions, where it can act as a catalyst or a reactant to facilitate novel synthetic pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 6265-95-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6265-95:
(6*6)+(5*2)+(4*6)+(3*5)+(2*9)+(1*5)=108
108 % 10 = 8
So 6265-95-8 is a valid CAS Registry Number.

6265-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4Z)-4-(3H-1,3-benzothiazol-2-ylidene)-2-ethoxycyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 2-ethoxy-4-benzothiazol-2-yl-phenol

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:6265-95-8 SDS

6265-95-8Downstream Products

6265-95-8Relevant academic research and scientific papers

NOVEL COMPOUND HAVING SKIN-WHITENING, ANTI-OXIDIZING AND PPAR ACTIVITIES AND MEDICAL USE THEREFOR

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Paragraph 0151-0159; 0163, (2014/02/16)

Provided are a novel compound having skin-whitening, anti-oxidizing and PPAR activities and a medical use thereof, and the compound has skin-whitening activities for the suppression of tyrosinase, and accordingly, is useful for use in skin-whitening pharmaceutical composition or cosmetic products; has anti-oxidant activities, and accordingly, is useful for the prevention and treatment of skin-aging; and has PPAR activities, and in particular, PPARα and PPARγ activities, and accordingly, is useful for use in pharmaceutical compositions or health foods which are effective for the prevention and treatment of obesity, metabolic disease, or cardiovascular disease.

Synthesis and biological activity of hydroxy substituted phenyl-benzo[d]thiazole analogues for antityrosinase activity in B16 cells

Ha, Young Mi,Park, Ji Young,Park, Yun Jung,Park, Daeui,Choi, Yeon Ja,Kim, Ji Min,Lee, Eun Kyeong,Han, Yu Kyeong,Kim, Jin-Ah,Lee, Ji Yeon,Moon, Hyung Ryong,Chung, Hae Young

supporting information; experimental part, p. 2445 - 2449 (2011/06/17)

In this study, we synthesized hydroxy and/or alkoxy substituted phenyl-benzo[d]thiazole derivatives using substituted benzaldehydes and 2-aminothiophenol in MeOH. The structures of these compounds were established by 1H and 13C NMR a

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