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(S)-N-(1-cyclopropylallyl)-4-methoxyaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1610792-96-5

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1610792-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1610792-96-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,7,9 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1610792-96:
(9*1)+(8*6)+(7*1)+(6*0)+(5*7)+(4*9)+(3*2)+(2*9)+(1*6)=165
165 % 10 = 5
So 1610792-96-5 is a valid CAS Registry Number.

1610792-96-5Upstream product

1610792-96-5Relevant academic research and scientific papers

Cobalt-Catalyzed Regio- and Enantioselective Allylic Amination

Ghorai, Samir,Chirke, Sahadev Shrihari,Xu, Wen-Bin,Chen, Jia-Feng,Li, Changkun

, p. 11430 - 11434 (2019)

The first earth-abundant cobalt-catalyzed highly branched- and enantioselective allylic amination of racemic branched allylic carbonates bearing alkyl groups with both aromatic and aliphatic amines has been developed. The process allows rapid access of allylic amines in high yields with exclusively branched selectivity and excellent enantioselectivities (normally 99% ee) under mild reaction conditions.

Rh(I)/Bisoxazolinephosphine-Catalyzed Regio- And Enantioselective Allylic Substitutions

Ghorai, Samir,Huang, Wenyu,Li, Changkun,Xu, Wen-Bin

, p. 4491 - 4496 (2020/05/19)

Rhodium(I)/bisoxazolinephosphine combination has been developed as a general catalyst to achieve the dynamic kinetic asymmetric allylation of a variety of nitrogen, carbon, oxygen, and sulfur pronucleophiles from branched racemic allylic carbonates. Exclusive branch-selectivity and up to 99% enantiomeric excess could be obtained under neutral conditions. Linear allylic substrates (both Z and E) could be converted to the same chiral branched products with excellent regio- and enantioselectivities as well. Chiral π-allyl-Rh(III)/NPN intermediate was isolated and characterized to understand the origin of the high selectivities.

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