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(E)-4-(2-(benzo[d][1,3]dioxol-5-yl)vinyl)benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1374418-58-2

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1374418-58-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374418-58-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,4,1 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1374418-58:
(9*1)+(8*3)+(7*7)+(6*4)+(5*4)+(4*1)+(3*8)+(2*5)+(1*8)=172
172 % 10 = 2
So 1374418-58-2 is a valid CAS Registry Number.

1374418-58-2Downstream Products

1374418-58-2Relevant academic research and scientific papers

Discovery of efficient stimulators for adult hippocampal neurogenesis based on scaffolds in dragon's blood

Liang, Jian-Hua,Yang, Liang,Wu, Si,Liu, Si-Si,Cushman, Mark,Tian, Jing,Li, Nuo-Min,Yang, Qing-Hu,Zhang, He-Ao,Qiu, Yun-Jie,Xiang, Lin,Ma, Cong-Xuan,Li, Xue-Meng,Qing, Hong

supporting information, p. 382 - 392 (2017/05/19)

Reduction of hippocampal neurogenesis caused by aging and neurological disorders would impair neural circuits and result in memory loss. A new lead compound (N-trans-3′,4'-methylenedioxystilben-4-yl acetamide 27) has been discovered to efficiently stimulate adult rats' neurogenesis. In-depth structure-activity relationship studies proved the necessity of a stilbene scaffold that is absent in highly cytotoxic analogs such as chalcones and heteroaryl rings and inactive analogs such as diphenyl acetylene and diphenyl ethane, and validated the importance of an NH in the carboxamide and a methylenedioxy substituent on the benzene ring. Immunohistochemical staining and biochemical analysis indicate, in contrast to previously reported neuroprotective chemicals, N-stilbenyl carboxamides have extra capacity for neuroproliferation-type neurogenesis, thereby providing a foundation for improving the plasticity of the adult mammalian brain.

Palladium-catalyzed dehydrative Heck olefination of secondary aryl alcohols in ionic liquids: Towards a waste-free strategy for tandem synthesis of stilbenoids

Kumar, Rakesh,Shard, Amit,Bharti, Richa,Thopate, Yogesh,Sinha, Arun Kumar

supporting information; experimental part, p. 2636 - 2639 (2012/04/17)

All in one: A tandem strategy has been developed wherein secondary aryl alcohols are directly coupled with aryl halides to provide stilbenoids through a dehydrative Heck sequence in the ionic liquid [hmim]Br, and with water as a by-product under microwave irradiation (see scheme). Classical methods do not permit this sequence to proceed in one pot, and some methods require multiple steps. hmim=1-n-hexyl-3-methylimidazolium. Copyright

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