Cas 1355024-83-7,1-tert-butyl 2-methyl 5-hydroxy-4-(3,4,5-trimethoxyphenethyl)-5,6-dihydropyrazine-1,2(4H)-dicarboxylate

1355024-83-7

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Basic information

Product Name: 1-tert-butyl 2-methyl 5-hydroxy-4-(3,4,5-trimethoxyphenethyl)-5,6-dihydropyrazine-1,2(4H)-dicarboxylate
Synonyms: 1-tert-butyl 2-methyl 5-hydroxy-4-(3,4,5-trimethoxyphenethyl)-5,6-dihydropyrazine-1,2(4H)-dicarboxylate
CAS NO:1355024-83-7
Molecular Formula:
Molecular Weight: 452.505
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: 1-tert-butyl 2-methyl 5-hydroxy-4-(3,4,5-trimethoxyphenethyl)-5,6-dihydropyrazine-1,2(4H)-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: 1-tert-butyl 2-methyl 5-hydroxy-4-(3,4,5-trimethoxyphenethyl)-5,6-dihydropyrazine-1,2(4H)-dicarboxylate(1355024-83-7)
EPA Substance Registry System: 1-tert-butyl 2-methyl 5-hydroxy-4-(3,4,5-trimethoxyphenethyl)-5,6-dihydropyrazine-1,2(4H)-dicarboxylate(1355024-83-7)

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: 1355024-83-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1355024-83-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,5,0,2 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1355024-83:
(9*1)+(8*3)+(7*5)+(6*5)+(5*0)+(4*2)+(3*4)+(2*8)+(1*3)=137
137 % 10 = 7
So 1355024-83-7 is a valid CAS Registry Number.

1355024-83-7Upstream product

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1355024-83-7Relevant academic research and scientific papers

Diversity-oriented synthesis of polycyclic diazinic scaffolds

Gigant, Nicolas,Claveau, Elise,Bouyssou, Pascal,Gillaizeau, Isabelle

supporting information; experimental part, p. 844 - 847 (2012/03/26)

An efficient and versatile synthesis of a polycyclic diazinic system starting from oxazine has been developed using a two-step Michael/retro Michael and cyclization sequence. The substrates were synthesized with good to high yields giving rapid access to molecular diversity.

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