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N-ethyl-7-methyl-7H-purin-6-amine, also known as 7-ethyl-7-methylguanine, is an organic compound belonging to the purine family. It is a derivative of guanine, a fundamental component of nucleic acids like DNA and RNA. N-ethyl-7-methyl-7H-purin-6-amine features a guanine molecule with an ethyl group attached to the nitrogen atom at position 7 and a methyl group at the same position. It is characterized by its molecular formula C8H11N5 and a molecular weight of 179.21 g/mol. The compound is of interest in medicinal chemistry, particularly in the study of nucleoside analogs, which can be used as antiviral and anticancer agents. Its structure and properties make it a potential candidate for the development of new therapeutics targeting nucleic acid metabolism.

5470-51-9

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5470-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5470-51-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,7 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5470-51:
(6*5)+(5*4)+(4*7)+(3*0)+(2*5)+(1*1)=89
89 % 10 = 9
So 5470-51-9 is a valid CAS Registry Number.

5470-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2Cl-N(6)-cPen-1-deaza-A

1.2 Other means of identification

Product number -
Other names 1-Dcca

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:5470-51-9 SDS

5470-51-9Downstream Products

5470-51-9Relevant academic research and scientific papers

7,9-Dialkyladeninium salts. An alternative synthesis, ring opening, and rearrangement to N6,7-dialkyladenines

Fujii, Tozo,Saito, Tohru,Inoue, Isao

, p. 909 - 913 (2007/10/02)

Alkylation of N1-alkoxy-1-alkyl-5-formamidoimidazole-4-carboxamidine (type I or II) (in the absence of any base) followed by hydrogenolysis of the N1-alkoxy group and cyclization (or vice versa) yielded the corresponding 7,9-dialkyladeninium salts (type VII), which readily rearranged to N6,7-dialkyladenines (type X) in boiling 1 N NaOH.Under milder basic conditions, VII underwent hydrolysis to produce 4-alkylamino-6-amino-5-formamidopyrimidines (VIII).The NaBH4 reduction of 7,9-dimethyladeninium iodide (VIIa, X=I) gave the 7,8-dihydro derivative (XI)

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