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893620-41-2

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893620-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 893620-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,3,6,2 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 893620-41:
(8*8)+(7*9)+(6*3)+(5*6)+(4*2)+(3*0)+(2*4)+(1*1)=192
192 % 10 = 2
So 893620-41-2 is a valid CAS Registry Number.

893620-41-2Downstream Products

893620-41-2Relevant articles and documents

Nickel-Catalyzed Intramolecular Hydroalkenylation of Imines

Feng, Wei-Min,Li, Tian-Yu,Xiao, Li-Jun,Zhou, Qi-Lin

supporting information, p. 7900 - 7904 (2021/10/12)

A ligand-enabled nickel-catalyzed intramolecular hydroalkenylation of imines with unactivated alkenes has been developed. A variety of five- and six-membered cyclic allylic amines were synthesized in high yields. The use of both wide-bite-angle diphosphine ligand and Br?nsted acid is crucial for realizing the reaction. Preliminary investigation of the asymmetric intramolecular hydroalkenylation of imines shows promising potential for the application of the method in the synthesis of enantio-enriched cyclic allylic amines.

Visible-Light-Induced Tandem Radical Addition-Cyclization of Alkenyl Aldehydes Leading to Indanones and Related Compounds

Lu, Danyang,Wan, Yimei,Kong, Lichun,Zhu, Gangguo

supporting information, p. 2929 - 2932 (2017/06/07)

Herein we describe a novel, visible light-induced tandem radical addition-cyclization of alkenyl aldehydes with α-bromocarbonyl compounds. A set of cyclic ketones, including indanones, cyclopentenones, 3,4-dihydronaphthalen-1(2H)-ones, and chroman-4-ones,

Direct intramolecular conjugate addition of simple alkenes to α,β-unsaturated carbonyls catalyzed by Cu(OTf)2

Qin, Yan,Lv, Jian,Luo, Sanzhong,Cheng, Jin-Pei

supporting information, p. 5032 - 5035 (2014/12/11)

An unprecedented intramolecular conjugate addition of simple alkenes to α,β-unsaturated carbonyl compounds has been developed. A simple Lewis acid such as Cu(OTf)2 was found to effectively catalyze the reaction, and six- and five-membered cycli

Synthesis of five- and six-membered benzocyclic ketones through intramolecular alkene hydroacylation catalyzed by Nickel(0)/N-Heterocyclic Carbenes

Hoshimoto, Yoichi,Hayashi, Yukari,Suzuki, Haruka,Ohashi, Masato,Ogoshi, Sensuke

, p. 10812 - 10815 (2013/01/15)

Getting some closure: Mechanistic studies supported the participation of an oxanickelacycle complex in the hydroacylation step of the title reaction, which proceeds without decarbonylation even in the absence of well-known chelation assistance by heteroatoms. Copyright

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