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(5-chloropent-1-ene-1,1-diyl)dibenzene, also known as 1,1'-(5-chloropent-1-ene-1,1-diyl)bisbenzene, is an organic compound with the molecular formula C15H15Cl. It is a colorless to pale yellow crystalline solid that is insoluble in water but soluble in organic solvents. (5-chloropent-1-ene-1,1-diyl)dibenzene is characterized by the presence of a 5-chloropent-1-ene-1,1-diyl group, which connects two benzene rings. The chloro substituent on the pentene group imparts unique chemical properties to the molecule, making it a potential intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and the presence of a halogen, it is important to handle (5-chloropent-1-ene-1,1-diyl)dibenzene with care, following appropriate safety protocols.

7035-13-4

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7035-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7035-13-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,3 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7035-13:
(6*7)+(5*0)+(4*3)+(3*5)+(2*1)+(1*3)=74
74 % 10 = 4
So 7035-13-4 is a valid CAS Registry Number.

7035-13-4Relevant academic research and scientific papers

Alkenylation of unactivated alkyl bromides through visible light photocatalysis

Zhou, Quan-Quan,Düsel, Simon Josef Siegfried,Lu, Liang-Qiu,K?nig, Burkhard,Xiao, Wen-Jing

, p. 107 - 110 (2019)

Two visible-light driven alkenylation reactions of unactivated alkyl bromides, which were enabled by the use of Ir(dF(CF3)ppy)2(dtbbpy)PF6 as the photocatalyst and (TMS)3SiH as the atom transfer reagent to activate the alkyl bromides, were described for the first time. These protocols can be used to produce a variety of alkenes from easily available feedstock with good reaction efficiency and high chemoselectivity under mild reaction conditions. To further demonstrate the applicability of the present strategy, the alkenylation of bioactive molecules and glycosyl bromides, as well as the alkynylation of unactivated alkyl bromides, was proven to be feasible.

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