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N-(3-methyl-1-phenylbut-3-en-1-yl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

443754-46-9

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443754-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 443754-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,7,5 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 443754-46:
(8*4)+(7*4)+(6*3)+(5*7)+(4*5)+(3*4)+(2*4)+(1*6)=159
159 % 10 = 9
So 443754-46-9 is a valid CAS Registry Number.

443754-46-9Downstream Products

443754-46-9Relevant academic research and scientific papers

Copper-Catalyzed Umpolung of Imines through Carbon-to-Nitrogen Boryl Migration

Li, Zhenghua,Zhang, Liang,Nishiura, Masayoshi,Hou, Zhaomin

, p. 4388 - 4393 (2019/05/08)

We report a general strategy for the catalytic umpolung of imines, which was enabled by an unprecedented 1,2-boryl carbon-to-nitrogen migration. Based on the discovery of a rearrangement of an α-borylalkylamido copper intermediate to an α-borylaminoalkyl

Synthesis of substituted γ-lactam via Pd(0)-catalyzed cyclization of alkene-tethered carbamoyl chloride

Chen, Chen,Hu, Jian,Su, Jianhua,Tong, Xiaofeng

supporting information, p. 3229 - 3231 (2014/06/09)

Pd(0)-catalyzed carboiodonation of but-3-enylcarbamic chloride has been developed with NaI as additive, which provides a ready access to substituted γ-lactam bearing an alkyl iodide group. This reaction features alkyl iodide reductive elimination as a key step in catalytic cycle, indicating the crucial role of additive NaI.

Bu4N+ alkoxide-initiated/autocatalytic addition reactions with organotrimethylsilanes

Das, Manas,O'Shea, Donal F.

, p. 5595 - 5607 (2014/07/08)

The use of Me3SiO-/Bu4N+ as a general activator of organotrimethylsilanes for addition reactions has been established. The broad scope of the method offers trimethylsilanes (including acetate, allyl, propargyl, benzyl, dithiane, heteroaryl, and aryl derivatives) as bench-stable organometallics that can be readily utilized as carbanion equivalents for synthesis. Reactions are achieved at rt without the requirement of specialized precautions that are commonplace for other organometallics.

Allyl-, allenyl-, and propargyl-transfer reactions through cleavage of C-C bonds catalyzed by an n-heterocyclic carbene/copper complex: Synthesis of multisubstituted pyrroles

Sai, Masahiro,Yorimitsu, Hideki,Oshima, Koichiro

supporting information; scheme or table, p. 3294 - 3298 (2011/06/21)

Cat. in the bag: The pictured copper complex can promote C-C bond cleavage through retro-allylation of homoallyl alcohols to form allylcopper species. This process is applicable to catalytic allylation of aldehydes and imines with homoallyl alcohols. The method has also been extended to regioselective allenylation and propargylation of imines. Copyright

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