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The chemical compound "(3aR,4R,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carbonitrile" is a complex organic molecule with a non-preferred name. It features a tetrahydrofuro[3,4-d][1,3]dioxole ring system, which is a type of cyclic ether, and a 6-amino-9H-purin-9-yl group, indicating the presence of a purine moiety, a key component in nucleic acids. The compound also includes a carbonitrile group, suggesting the presence of a nitrile functional group. This molecule is characterized by its specific stereochemistry, with the 3aR, 4R, 6R, and 6aR configurations, which define the spatial arrangement of its atoms. The compound's structure and properties make it a potential candidate for various applications in medicinal chemistry and pharmaceutical research, particularly in the development of nucleoside analogs and other therapeutic agents.

54918-23-9

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54918-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54918-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,1 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54918-23:
(7*5)+(6*4)+(5*9)+(4*1)+(3*8)+(2*2)+(1*3)=139
139 % 10 = 9
So 54918-23-9 is a valid CAS Registry Number.

54918-23-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3aR,4R,6R,6aR)-4-(6-aminopurin-9-yl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxole-6-carbonitrile

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:54918-23-9 SDS

54918-23-9Downstream Products

54918-23-9Relevant academic research and scientific papers

A simple synthesis of nitriles from aldoximes

Singh, Manish K.,Lakshman, Mahesh K.

experimental part, p. 3079 - 3084 (2009/08/08)

Easily synthesized aldoximes have been converted to the corresponding nitriles under very mild conditions by a simple reaction with lH-benzotriazol-l-yloxytris(dimethylamino)phosphonium hexafluorophosphate (BOP) and DBU in CH2CI2, THF, or DMF. As an alternative reagent that eliminates the formation of hexamethylphosphoramide as a byproduct, use of lH-benzotriazol-lyl-4-methylbenzenesulfonate (Bt-OTs) and DBU was investigated. Reactions with this reagent also proceeded smoothly and in good yields, although in one case N-sulfonylation was observed. An attempt to gain mechanistic insight into the BOP-mediated reaction has been made using 31P{ 1H} NMR. However, no phosphorus-bearing intermediate could be readily observed. Finally, the method has been applied to the synthesis of an antiviral 4'-cyano adenosine analogue from a commercial precursor using a single saccharide protecting group.

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