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3-Buten-2-ol, 2-methyl-4-(4-methylphenyl)-, (3Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

334875-18-2

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334875-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 334875-18-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,4,8,7 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 334875-18:
(8*3)+(7*3)+(6*4)+(5*8)+(4*7)+(3*5)+(2*1)+(1*8)=162
162 % 10 = 2
So 334875-18-2 is a valid CAS Registry Number.

334875-18-2Relevant academic research and scientific papers

Aqueous phase semihydrogenation of alkynes over Ni-Fe bimetallic catalysts

Awasthi, Mahendra K.,Barman, Sudipta Roy,Behrens, Silke,Rai, Rohit K.,Singh, Sanjay K.,Singh, Vipin K.

, p. 4968 - 4980 (2020/08/19)

Bimetallic Ni-Fe catalysts (Ni/Fe, 1?:?1, 1?:?3, and 3?:?1) are synthesized and explored for their catalytic activity in semihydrogenation of internal alkynes using H2 gas in water-ethanol solution. Our findings revealed that over the Ni1Fe3 catalyst a high diastereoselectivity for Z-alkenes with a high conversion for a wide range of internal alkynes can be achieved at moderate reaction temperature (40 °C). Notably, the selectivity for the Z-alkenes is enhanced in the presence of n-butyl amine as an additive. Deuterium labeling experiments evidenced that H2 gas becomes dissociated homolytically over the catalyst surface to hydrogenate alkynes to alkenes. Synthesized catalysts were successfully characterized by HR-TEM, SEM, XPS, EDS, P-XRD and H2-TPD.

Reactions of vinyltributylgermanes and aryl halides under Heck conditions

Torres, Nicole M.,Lavis, Jér?me M.,Maleczka Jr., Robert E.

experimental part, p. 4407 - 4410 (2009/10/26)

We describe the palladium-mediated reaction of vinyltributylgermanes with aryl halides under Heck conditions. Depending on their degree of substitution, (E)-vinyltributylgermanes preferentially afford either the cine or Z-alkenyl coupled products in moder

Highly activated vinyl hydrogen in a significantly twisted styrene

Mori, Hajime,Matsuo, Takafumi,Yoshioka, Yasunori,Katsumura, Shigeo

, p. 9004 - 9012 (2007/10/03)

(Chemical Equation Presented) The novel example of a vinylic hydrogen more reactive than a benzylic hydrogen was found by treatment of a twisted styrene derivative with a strong base followed by D2O quenching. In this paper, the full details of

Vinyl hydrogen more reactive than benzyl hydrogen toward base in significantly twisted styrenes

Mori, Hajime,Matsuo, Takafumi,Yoshioka, Yasunori,Katsumura, Shigeo

, p. 3093 - 3095 (2007/10/03)

The novel example of vinyl hydrogen more reactive than benzylic hydrogen was found by treatment of a twisted styrene derivative with a strong base followed by D2O quenching. The characteristic nature of the vinyl hydrogen, which is activated by

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