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Benzene,1,1'-(1,3,5,7,9-decapentaene-1,10-diyl)bisis a chemical compound that consists of a benzene ring with a bridge of 1,1'-(1,3,5,7,9-decapentaene-1,10-diyl)bis-. It is a type of polyene, meaning it contains multiple double bonds in its structure. The unique structure of Benzene,1,1'-(1,3,5,7,9-decapentaene-1,10-diyl)bis- makes it a potentially valuable building block for the creation of new materials and pharmaceuticals.

3029-41-2

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3029-41-2 Usage

Uses

Used in Organic Chemistry:
Benzene,1,1'-(1,3,5,7,9-decapentaene-1,10-diyl)bisis used as a precursor for the synthesis of other compounds due to its polyene structure.
Used in Materials Science:
Benzene,1,1'-(1,3,5,7,9-decapentaene-1,10-diyl)bisis used as a building block for the creation of new materials, taking advantage of its unique structure.
Used in Pharmaceutical Research:
Benzene,1,1'-(1,3,5,7,9-decapentaene-1,10-diyl)bisis used in pharmaceutical research for its potential applications in the development of new drugs.
Used in Chemical Industry:
It is used as a component in the production of various chemical products, leveraging its properties as a polyene.
It is important to handle Benzene,1,1'-(1,3,5,7,9-decapentaene-1,10-diyl)biswith care, as benzene and polyenes are known to be hazardous to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 3029-41-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,2 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3029-41:
(6*3)+(5*0)+(4*2)+(3*9)+(2*4)+(1*1)=62
62 % 10 = 2
So 3029-41-2 is a valid CAS Registry Number.

3029-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [(1E,3E,5E,7E,9E)-10-phenyldeca-1,3,5,7,9-pentaenyl]benzene

1.2 Other means of identification

Product number -
Other names 1,10-Diphenyl-deca-1,3,5,7,9-pentaen

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:3029-41-2 SDS

3029-41-2Downstream Products

3029-41-2Relevant academic research and scientific papers

Palladium-Catalyzed Syntheses of Aryl Polyenes

Mitsudo, Taki-aki,Fischetti, William,Heck, Richard F.

, p. 1640 - 1646 (2007/10/02)

The palladium-catalyzed arylation reaction has been employed to prepare a variety of mono- and diaryl 1,3-dienes and 1,3,5-trienes.The yields were good when electron withdrawing substituents were present in the aryl groups but only poor to fair when electron-donating groups were involved.Monoaryl dienes and trienes reacted well with all types of aryl halides to give mixed diaryl derivatives. 2-Bromostyrene reacts with phenylhexatriene to form 1,8-diphenyloctatetraene and with hexatriene to form 1,10-diphenyldecapentaene, but both only in about 15percent yield.

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