Cas 231629-79-1,6-t-butyl-4-benzyl-4,9-dihydro-3-[(2-hydroxyethoxy)methyl]-9-oxo-3H-imidazo[1,2-a]purine

231629-79-1

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Basic information

Product Name: 6-t-butyl-4-benzyl-4,9-dihydro-3-[(2-hydroxyethoxy)methyl]-9-oxo-3H-imidazo[1,2-a]purine
Synonyms:
CAS NO:231629-79-1
Molecular Formula:
Molecular Weight: 395.461
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: 6-t-butyl-4-benzyl-4,9-dihydro-3-[(2-hydroxyethoxy)methyl]-9-oxo-3H-imidazo[1,2-a]purine(CAS DataBase Reference)
NIST Chemistry Reference: 6-t-butyl-4-benzyl-4,9-dihydro-3-[(2-hydroxyethoxy)methyl]-9-oxo-3H-imidazo[1,2-a]purine(231629-79-1)
EPA Substance Registry System: 6-t-butyl-4-benzyl-4,9-dihydro-3-[(2-hydroxyethoxy)methyl]-9-oxo-3H-imidazo[1,2-a]purine(231629-79-1)

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: 231629-79-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 231629-79-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,1,6,2 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 231629-79:
(8*2)+(7*3)+(6*1)+(5*6)+(4*2)+(3*9)+(2*7)+(1*9)=131
131 % 10 = 1
So 231629-79-1 is a valid CAS Registry Number.

231629-79-1Upstream product

231629-79-1Downstream Products

231629-90-6 3-benzyl-9-[(2-hydroxyethoxy)methyl]guanine

231629-79-1Relevant academic research and scientific papers

Substituent-directed aralkylation and alkylation reactions of the tricyclic analogues of acyclovir and guanosine

Ostrowski,Zeidler,Goslinski,Golankiewicz

, p. 1911 - 1929 (2007/10/03)

Aryl or tert-butyl substituent in the 6 position of 3,9-dihydro-3-[(2-hydroxyethoxy)methyl]-9-oxo-6-R-5H-imidazo[1,2-a]purine (6-R-TACV)11 partly directs aralkylation reactions into unusual positions: N-4 to give 3 and C-7 to give N-5,7-disubst

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