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3-Chlor-1-(3-chlor-phenyl)-prop-1-en, also known as 3-chloro-1-(3-chlorophenyl)prop-1-en or 3-chloro-1-(3-chlorophenyl)propene, is an organic compound with the chemical formula C9H8Cl2. It is a colorless liquid with a molecular weight of 197.07 g/mol. 3-Chlor-1-(3-chlor-phenyl)-prop-1-en is characterized by the presence of a propene backbone, with one chlorine atom attached to the propene's carbon chain and another chlorine atom on the phenyl ring. It is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive nature, it is typically handled under controlled conditions to prevent unwanted side reactions or hazards.

1507-91-1

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1507-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1507-91-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1507-91:
(6*1)+(5*5)+(4*0)+(3*7)+(2*9)+(1*1)=71
71 % 10 = 1
So 1507-91-1 is a valid CAS Registry Number.

1507-91-1Downstream Products

1507-91-1Relevant academic research and scientific papers

Multifunctional novel Diallyl disulfide (DADS) derivatives with β-amyloid-reducing, cholinergic, antioxidant and metal chelating properties for the treatment of Alzheimer's disease

Manral, Apra,Saini, Vikas,Meena, Poonam,Tiwari, Manisha

, p. 6389 - 6403 (2015/10/05)

A series of novel Diallyl disulfide (DADS) derivatives were designed, synthesized and evaluated as chemical agents, which target and modulate multiple facets of Alzheimer's disease (AD). The results showed that the target compounds 5a-l and 7e-m exhibited significant anti-Aβ aggregation activity, considerable acetylcholinesterase (AChE) inhibition, high selectivity towards AChE over butyrylcholinesterase (BuChE), potential antioxidant and metal chelating activities. Specifically, compounds 7k and 7l exhibited highest potency towards self-induced Aβ aggregation (74% and 71.4%, 25 μM) and metal chelating ability. Furthermore, compounds 7k and 7l disaggregated Aβ fibrils generated by Cu2+-induced Aβ aggregation by 80.9% and 78.5%, later confirmed by transmission electron microscope (TEM) analysis. Besides, 7k and 7l had the strongest AChE inhibitory activity with IC50 values of 0.056 μM and 0.121 μM, respectively. Furthermore, molecular modelling studies showed that these compounds were capable of binding simultaneously to catalytic active site (CAS) and peripheral anionic site (PAS) of AChE. All the target compounds displayed moderate to excellent antioxidant activity with ORAC-FL values in the range 0.546-5.86 Trolox equivalents. In addition, absorption, distribution, metabolism and excretion (ADME) profile and toxicity prediction (TOPKAT) of best compounds 7k and 7l revealed that they have drug like properties and possess very low toxic effects. Collectively, the results strongly support our assertion that these compounds could provide good templates for developing new multifunctional agents for AD treatment.

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