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476493-40-0

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476493-40-0 Usage

Uses

1-N-Boc-3-cyanopyrrolidine is used to prepare aroyl-substituted pyrrolidines with monoamine reuptake inhibition activities.

Check Digit Verification of cas no

The CAS Registry Mumber 476493-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,6,4,9 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 476493-40:
(8*4)+(7*7)+(6*6)+(5*4)+(4*9)+(3*3)+(2*4)+(1*0)=190
190 % 10 = 0
So 476493-40-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H16N2O2/c1-10(2,3)14-9(13)12-5-4-8(6-11)7-12/h8H,4-5,7H2,1-3H3

476493-40-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H50082)  1-Boc-3-cyanopyrrolidine, 99%   

  • 476493-40-0

  • 250mg

  • 867.0CNY

  • Detail
  • Alfa Aesar

  • (H50082)  1-Boc-3-cyanopyrrolidine, 99%   

  • 476493-40-0

  • 1g

  • 3117.0CNY

  • Detail

476493-40-0Relevant articles and documents

NOVEL COMPOUNDS FOR INHIBITION OF JANUS KINASE 1

-

Page/Page column 90, (2020/12/11)

An object of the invention is to provide compounds as selective JAK1 inhibitor, a process for preparation of the inhibitors, a composition containing the compounds and utility of the compounds.

Glutaminase inhibitors as well as compositions and applications thereof

-

, (2018/01/09)

The invention provides a series of heterocyclic compounds expressed in a formula I. The compound comprises glutaminase inhibition activity, and can be used for treating diseases and symptoms related to dysfunction of glutaminase or raising activity of glutaminase.

Visible-Light-Mediated Alkenylation, Allylation, and Cyanation of Potassium Alkyltrifluoroborates with Organic Photoredox Catalysts

Heitz, Drew R.,Rizwan, Komal,Molander, Gary A.

, p. 7308 - 7313 (2016/08/30)

Iridium- and ruthenium-free approaches to protected allylic amines and alkyl nitriles under photoredox conditions are reported. An inexpensive organic dye, eosin Y, catalyzes coupling of Boc-protected potassium α-aminomethyltrifluoroborates with a variety of substituted alkenyl sulfones through an α-aminomethyl radical addition-elimination pathway. Allylic and homoallylic amines were formed in moderate yields with high E/Z selectivity. The mechanistic approach was extended using tosyl cyanide as a radical trap, enabling the conversion of alkyltrifluoroborates to nitriles via a Fukuzumi acridinium-catalyzed process.

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