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"9H-Purine-9-acetic acid, 6-(benzoylamino)-, ethyl ester" is a complex organic compound with the chemical formula C18H18N4O3. It is a derivative of purine, a heterocyclic aromatic organic compound that is a component of nucleic acids. This specific compound features a purine core with an acetic acid group at the 9-position, a benzoylamine group at the 6-position, and an ethyl ester group. It is known for its potential applications in medicinal chemistry, particularly in the development of drugs targeting adenosine receptors, which are involved in various physiological processes including cardiovascular function, neuroprotection, and immune response modulation. The compound's structure and properties make it a subject of interest for researchers exploring new therapeutic strategies.

171406-46-5

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171406-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 171406-46-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,4,0 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 171406-46:
(8*1)+(7*7)+(6*1)+(5*4)+(4*0)+(3*6)+(2*4)+(1*6)=115
115 % 10 = 5
So 171406-46-5 is a valid CAS Registry Number.

171406-46-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(6-benzamidopurin-9-yl)acetate

1.2 Other means of identification

Product number -
Other names N6-Benzoyl-9-ethoxycarbonylmethyladenine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:171406-46-5 SDS

171406-46-5Relevant academic research and scientific papers

Acyclic nucleoside and nucleotide analogues with amide bond

Efimtseva,Mikhailov,Jasko,Malakhov,Semizarov,Fomicheva,Kern

, p. 373 - 375 (1995)

A series of acyclic nucleosides and related α-phosphonyl acyclic analogues of dNTP with an amide bond have been prepared. Their antiviral and substrate properties were investigated.

PEPTIDE NUCLEIC ACID MONOMERS AND OLIGOMERS

-

, (2011/10/13)

Disclosed is a peptide nucleic acid monomer as well as a corresponding peptide nucleic acid molecule. The monomer comprises a terminal amino group and a terminal group A. The terminal amino group and the terminal group A are connected by an aliphatic moie

Building blocks for Polyamide Nucleic Acids: Facile synthesis using potassium fluoride doped natural phosphate as basic catalyst

Alahiane,Taourirte,Rochdi,Redwane,Sebti,Engels,Lazrek

, p. 109 - 114 (2007/10/03)

Potassium fluoride doped natural phosphate, inexpensive and environmentally friendly catalyst, is shown to be an efficient basic catalyst for the N1/N9 alkylation of different nucleobases as synthons for PNAs.

Synthesis and Biochemical Properties of Phosphonyl Acyclic Analogs of 2'Deoxyadenosine Nucleotides

Malakhov, D. V.,Semizarov, D. G.,Yas'ko, M. V.

, p. 464 - 469 (2007/10/03)

9-adenine, 9-adenine, 9-ethyl>adenine, and their diphosphates were synthesized.All three diphosphates were shown to incorporate into the 3'-te

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