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1-[4-(5-Bromo-pentyloxy)-3-methoxy-phenyl]-ethanone is a complex organic compound with the molecular formula C14H19BrO3. It is characterized by a phenyl ring with a bromine atom attached to the pentyloxy chain, which is connected to the phenyl ring at the para position. The phenyl ring also has a methoxy group at the ortho position. 1-[4-(5-Bromo-pentyloxy)-3-methoxy-phenyl]-ethanone is a derivative of acetophenone, with the ethanone group (a ketone) attached to the phenyl ring. It is likely to be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and functional groups.

3510-63-2

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3510-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3510-63-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3510-63:
(6*3)+(5*5)+(4*1)+(3*0)+(2*6)+(1*3)=62
62 % 10 = 2
So 3510-63-2 is a valid CAS Registry Number.

3510-63-2Downstream Products

3510-63-2Relevant academic research and scientific papers

Design, synthesis and biological evaluation of rasagiline-clorgyline hybrids as novel dual inhibitors of monoamine oxidase-B and amyloid-β aggregation against Alzheimer's disease

Cheng, Maojun,Guo, Jie,Jiang, Neng,Li, Qing,Liang, Ningsheng,Liu, Jing,Nong, Xiaojie,Pang, Chengyun,Qin, Yuelian,Tang, Chunli,Tang, Weizhong,Xie, Sai-Sai,Zhang, Zhipeng

, (2020)

A series of rasagiline-clorgyline hybrids was designed, synthesized and investigated in vitro for their inhibition of monoamine oxidase and amyloid-β aggregation. Most of compounds were found to be selective and highly potent hMAO-B inhibitors showing IC50 values in the nanomolar, and exhibited a moderate inhibition of amyloid-β aggregation. 7-((5-(methyl(prop-2-yn-1-yl)amino) pentyl)oxy)chroman-4-one (6j) was the most interesting compound identified in this research, endowed with higher hMAO-B potency (IC50 = 4 nM) and selectivity (SI > 25000) compared to the reference selective inhibitor rasagiline (IC50 = 141 nM, SI > 355), and exhibited good inhibitory activity against Aβ1-42 aggregation (40.78percent, 25 μM). Kinetic and molecular modeling studies revealed that 6j was a competitive reversible inhibitor for hMAO-B. Moreover, compound 6j displayed low toxicity and good neuroprotective effects in SH-SY5Y cell assay, and could penetrate the blood-brain barrier according to the parallel artificial membrane permeability assay. Pharmacokinetics assay revealed that compound 6j possessed good pharmacokinetic profiles after intravenous and oral administrations. Overall, these results highlighted that compound 6j was an effective and promising multitarget agent against Alzheimer's disease.

Application of propynylamine derivative in pharmacy

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Paragraph 0046-0048, (2020/06/22)

The invention discloses application of a propynylamine derivative in pharmacy. Shown by tests of the applicant, the derivative can selectively inhibit MAO-B, is remarkable in activity and can be usedfor preparing MAO-B inhibitors and drugs for preventing

Propargylamine derivative and synthesis method thereof

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Paragraph 0037-0041, (2020/06/16)

The invention discloses a series of propargylamine derivatives and a synthesis method thereof. The synthesis method of the derivative mainly comprises the following steps: (1) putting any one of the structures shown in the following formulas (A)-(E) and e

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