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87259-89-0

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87259-89-0 Usage

General Description

"(1E,3E)-1,4-Bis(2-Nitrophenyl)Buta-1,3-Diene" is a chemical compound with the chemical formula C16H12N2O4. It is also known as 1,4-bis(2-nitrophenyl)buta-1,3-diene and belongs to the class of organic compounds known as nitrobenzenes. (1E,3E)-1,4-Bis(2-Nitrophenyl)Buta-1,3-Diene is a yellow solid that is insoluble in water but soluble in organic solvents. It is primarily used as a dye and pigment and has applications in the production of various types of coatings and paints. (1E,3E)-1,4-Bis(2-Nitrophenyl)Buta-1,3-Diene is also used in chemical research and as a building block for the synthesis of more complex organic compounds. It is important to handle and use this compound with care, as it can be harmful if ingested or inhaled and can cause skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 87259-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,5 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87259-89:
(7*8)+(6*7)+(5*2)+(4*5)+(3*9)+(2*8)+(1*9)=180
180 % 10 = 0
So 87259-89-0 is a valid CAS Registry Number.

87259-89-0SDS

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 1-nitro-2-[4-(2-nitrophenyl)buta-1,3-dienyl]benzene

1.2 Other means of identification

Product number -
Other names 1,4-Di-o-nitrophenyl-1,3-butadien

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:87259-89-0 SDS

87259-89-0Relevant articles and documents

Double Palladium Catalyzed Reductive Cyclizations. Synthesis of 2,2′-, 2,3′-, and 3,3′-Bi-1H-indoles, Indolo[3,2-b]indoles, and Indolo[2,3-b]indoles

Ansari, Nurul H.,Dacko, Christopher A.,Akhmedov, Novruz G.,S?derberg, Bj?rn C. G.

, p. 9337 - 9349 (2016/10/14)

A palladium catalyzed, carbon monoxide mediated, double reductive cyclization of 1,4-, 1,3-, and 2,3-bis(2-nitroaryl)-1,3-butadienes to afford 2,2′-, 2,3′-, and 3,3′-biindoles, respectively, was developed. In contrast, reductive cyclizations of 1,2-bis(2-nitroaryl)ethenes were nonselective, affording mixtures of monocyclized indoles, indolo[3,2-b]indole, indolo[1,2-c]quinazolin-6(5H)-ones, and 5,11-dihydro-6H-indolo[3,2-c]quinolin-6-ones. Nonselective product formation was also observed from reductive cyclization of 1,1-bis(2-nitroaryl)ethenes, producing indolo[2,3-b]indoles and indolo[2,3-c]quinolin-6-ones. Carbon monoxide insertion to give the carbonyl containing products was the major or sole reaction path starting from 1,1- or 1,2-bis(2-nitroaryl)ethenes.

The Total Synthesis of (+/-)K252a

Lowinger, Timothy B.,Chu, Jingxi,Spence, Patrick L.

, p. 8383 - 8386 (2007/10/02)

The total synthesis of (+/-)K252a (1) has been achieved following a convergent approach in which an acid-catalyzed bis-glycosidation reaction serves as a key step.

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