Cas 1365546-39-9,(2R,5R)-2-(2,5-dimethoxyphenyl)-5-isopropyl-3,6-dimethoxy-2-((6-methylpyridin-2-yl)methyl)-2,5-dihydropyrazine

1365546-39-9

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Basic information

Product Name: (2R,5R)-2-(2,5-dimethoxyphenyl)-5-isopropyl-3,6-dimethoxy-2-((6-methylpyridin-2-yl)methyl)-2,5-dihydropyrazine
Synonyms: (2R,5R)-2-(2,5-dimethoxyphenyl)-5-isopropyl-3,6-dimethoxy-2-((6-methylpyridin-2-yl)methyl)-2,5-dihydropyrazine
CAS NO:1365546-39-9
Molecular Formula:
Molecular Weight: 425.528
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2R,5R)-2-(2,5-dimethoxyphenyl)-5-isopropyl-3,6-dimethoxy-2-((6-methylpyridin-2-yl)methyl)-2,5-dihydropyrazine(CAS DataBase Reference)
NIST Chemistry Reference: (2R,5R)-2-(2,5-dimethoxyphenyl)-5-isopropyl-3,6-dimethoxy-2-((6-methylpyridin-2-yl)methyl)-2,5-dihydropyrazine(1365546-39-9)
EPA Substance Registry System: (2R,5R)-2-(2,5-dimethoxyphenyl)-5-isopropyl-3,6-dimethoxy-2-((6-methylpyridin-2-yl)methyl)-2,5-dihydropyrazine(1365546-39-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1365546-39-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1365546-39-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,5,5,4 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1365546-39:
(9*1)+(8*3)+(7*6)+(6*5)+(5*5)+(4*4)+(3*6)+(2*3)+(1*9)=179
179 % 10 = 9
So 1365546-39-9 is a valid CAS Registry Number.

1365546-39-9Upstream product

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1365546-39-9Relevant academic research and scientific papers

Asymmetric synthesis of quaternary aryl amino acid derivatives via a three-component aryne coupling reaction

Jones, Elizabeth P.,Jones, Peter,White, Andrew J. P.,Barrett, Anthony G. M.

supporting information; experimental part, p. 1570 - 1576 (2012/01/03)

A method was developed for the synthesis of α-alkyl, α-aryl-bislactim ethers in good to excellent yields and high diastereoselectivities, consisting of a facile one-pot procedure in which the aryl group is introduced by means of a nucleophilic addition to

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