Cas 1171072-06-2,1-tert-butyl 2-methyl 4-benzyl-5-(benzylamino)-5,6-dihydropyrazine-1,2(4H)-dicarboxylate

1171072-06-2

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Basic information

Product Name: 1-tert-butyl 2-methyl 4-benzyl-5-(benzylamino)-5,6-dihydropyrazine-1,2(4H)-dicarboxylate
Synonyms: 1-tert-butyl 2-methyl 4-benzyl-5-(benzylamino)-5,6-dihydropyrazine-1,2(4H)-dicarboxylate
CAS NO:1171072-06-2
Molecular Formula:
Molecular Weight: 437.539
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 4-benzyl-5-(benzylamino)-5,6-dihydropyrazine-1,2(4H)-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: 1-tert-butyl 2-methyl 4-benzyl-5-(benzylamino)-5,6-dihydropyrazine-1,2(4H)-dicarboxylate(1171072-06-2)
EPA Substance Registry System: 1-tert-butyl 2-methyl 4-benzyl-5-(benzylamino)-5,6-dihydropyrazine-1,2(4H)-dicarboxylate(1171072-06-2)

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: 1171072-06-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1171072-06-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,1,0,7 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1171072-06:
(9*1)+(8*1)+(7*7)+(6*1)+(5*0)+(4*7)+(3*2)+(2*0)+(1*6)=112
112 % 10 = 2
So 1171072-06-2 is a valid CAS Registry Number.

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1171072-06-2Relevant academic research and scientific papers

Reactivity of 5-hydroxy-5,6-dihydro-4H-pyrazines-easy and efficient access to ring-fused polycyclic diazinic systems

Claveau, Elise,Gillaizeau, Isabelle,Coudert, Gérard

supporting information; experimental part, p. 3679 - 3682 (2009/10/04)

An efficient synthesis of functionalized 1,4-diazinic hemiaminals starting from methyl-4H-1,4-oxazine-3-carboxylate moiety is reported. Given that various polycyclic heterocyclic frameworks could be easily obtained, this strategy may provide an efficient

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