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(2Z)-2-(diethylamino)-1,4-diphenylbut-2-ene-1,4-dione, also known as dibenzalacetone, is a yellow crystalline chemical compound with a wide range of applications and potential uses in various industries. It is commonly used in organic synthesis reactions and as a UV filter in sunscreen products. Dibenzalacetone has been studied for its potential anti-inflammatory and anti-cancer properties, and is also used as a reagent in the synthesis of various pharmaceutical and agrochemical compounds. (2Z)-2-(diethylamino)-1,4-diphenylbut-2-ene-1,4-dione is considered to be relatively stable and non-toxic when handled and used properly.

26454-87-5

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26454-87-5 Usage

Uses

Used in Organic Synthesis:
(2Z)-2-(diethylamino)-1,4-diphenylbut-2-ene-1,4-dione is used as a reagent in organic synthesis for the production of various compounds.
Used in Sunscreen Products:
(2Z)-2-(diethylamino)-1,4-diphenylbut-2-ene-1,4-dione is used as a UV filter in sunscreen products to protect the skin from harmful ultraviolet radiation.
Used in Pharmaceutical Industry:
(2Z)-2-(diethylamino)-1,4-diphenylbut-2-ene-1,4-dione is used as a reagent in the synthesis of various pharmaceutical compounds.
Used in Agrochemical Industry:
(2Z)-2-(diethylamino)-1,4-diphenylbut-2-ene-1,4-dione is used as a reagent in the synthesis of various agrochemical compounds.
Used in Anti-inflammatory Applications:
(2Z)-2-(diethylamino)-1,4-diphenylbut-2-ene-1,4-dione has been studied for its potential anti-inflammatory properties and may be used as an anti-inflammatory agent in the future.
Used in Anti-cancer Applications:
(2Z)-2-(diethylamino)-1,4-diphenylbut-2-ene-1,4-dione has been studied for its potential anti-cancer properties and may be used as an anti-cancer agent in the future.

Check Digit Verification of cas no

The CAS Registry Mumber 26454-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,5 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26454-87:
(7*2)+(6*6)+(5*4)+(4*5)+(3*4)+(2*8)+(1*7)=125
125 % 10 = 5
So 26454-87-5 is a valid CAS Registry Number.

26454-87-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-2-(diethylamino)-1,4-diphenylbut-2-ene-1,4-dione

1.2 Other means of identification

Product number -
Other names 3-Diaethylamino-1,4-diphenyl-2-buten-1,4-dion

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:26454-87-5 SDS

26454-87-5Relevant academic research and scientific papers

A 2-amino-butene 1,4-dione derivative synthesis method (by machine translation)

-

Paragraph 0039, (2017/03/14)

The invention belongs to the field of organic chemical and fine chemical industry, particularly relates to a preparation of 2-amino-butane -1,4-dione derivatives synthesis process. The benzoyl formaldehyde derivatives, and mixed terminal alkyne, joins the gold catalyst, reaction under heating condition, to obtain 2-amino-butane -1,4-dione derivatives, the yield is 62-85%. The reaction of the raw materials with a simple, one-pot synthesis is the synthesis of 2-amino-butane -1,4-dione derivatives, raw materials are all involved in the generation of the product, mild reaction conditions, has very high atom economy, for the synthesis of 2-amino-butane -1,4-dione derivatives provides a high-efficiency, green new synthesis method. (by machine translation)

Synthesis of 2-aminobutene-1,4-diones by gold-catalysed three-component coupling reactions

Liu, Li,Tang, Jiaqi,Qiang, Jian,He, Mingyang

, p. 247 - 249 (2016/05/19)

A gold-catalysed three-component coupling reaction of phenylglyoxal derivatives, alkynes and secondary amines was developed to provide a novel one-pot synthesis of 2-aminobutene-1,4-diones in moderate to good yields.

Substrate-controlled and highly stereoselective synthesis of 2-aminobut-2-ene-1, 4-diones

Deng, Cong,Yang, Yan,Gao, Meng,Zhu, Yan-Ping,Wu, An-Xin,Ma, Jun-Rui,Yin, Guo-Dong

, p. 3828 - 3834 (2012/07/02)

2-Methylthio-substituted 1,4-enediones, obtained from readily available aryl methyl ketones, were reacted with primary or secondary amines to afford the desired 1,4-diaryl-2-aminobut-2-ene-1,4-diones in excellent yields with high Z/E-stereoselectivity.

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