Cas 548943-40-4,N-[4-(5-hydroxy-2,4-dioxo-1,3-dipropyl-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-phenyl]-acetamide

548943-40-4

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Basic information

Product Name: N-[4-(5-hydroxy-2,4-dioxo-1,3-dipropyl-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-phenyl]-acetamide
Synonyms:
CAS NO:548943-40-4
Molecular Formula:
Molecular Weight: 384.435
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: N-[4-(5-hydroxy-2,4-dioxo-1,3-dipropyl-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-phenyl]-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[4-(5-hydroxy-2,4-dioxo-1,3-dipropyl-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-phenyl]-acetamide(548943-40-4)
EPA Substance Registry System: N-[4-(5-hydroxy-2,4-dioxo-1,3-dipropyl-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-phenyl]-acetamide(548943-40-4)

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: 548943-40-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 548943-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,8,9,4 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 548943-40:
(8*5)+(7*4)+(6*8)+(5*9)+(4*4)+(3*3)+(2*4)+(1*0)=194
194 % 10 = 4
So 548943-40-4 is a valid CAS Registry Number.

548943-40-4Upstream product

548943-40-4Downstream Products

1084328-31-3 6-(4-amino-phenyl)-5-hydroxy-1,3-dipropyl-1H-pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione

548943-40-4Relevant academic research and scientific papers

Fast and highly efficient one-pot synthesis of 9-deazaxanthines

Stefanachi, Angela,Leonetti, Francesco,Cappa, Anna,Carotti, Angelo

, p. 2121 - 2123 (2003)

SnCl2 enables a direct, high-yield conversion of 5-nitro-1,3-dialkyl-6-styryl(furyl-, thienyl-vinyl)-uracils to 8-substituted-9-deazaxanthines under very mild experimental conditions. The method has a general applicability and it is compatible with the reactivity of the most common organic functional groups. In slightly experimental different conditions, it allows a high-yield and fast (5 min) preparation of pure 7-N-hydroxy-9-deazaxanthines.

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