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2-Amino-9-(ethyl 2-carboethoxybutanoate-4-yl)purine is a complex-named chemical compound with the molecular formula C14H20N6O4. It is a derivative of purine, featuring an amino group and an ethyl carboethoxybutanoate substituent. As a synthetic compound, it holds potential in pharmaceuticals and medicine, particularly in cancer research and as a prospective drug target. 2-Amino-9-(ethyl 2-carboethoxybutanoate-4-yl)purine's specific properties and applications are under ongoing investigation, with its therapeutic potential yet to be fully realized.

122497-22-7

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122497-22-7 Usage

Uses

Used in Pharmaceutical Research:
2-Amino-9-(ethyl 2-carboethoxybutanoate-4-yl)purine is utilized as a research compound for its potential applications in the development of pharmaceuticals, especially in the field of cancer treatment. Its unique structure and properties make it a candidate for further exploration and possible drug design.
Used in Cancer Research:
In the field of cancer research, 2-Amino-9-(ethyl 2-carboethoxybutanoate-4-yl)purine is used as a potential drug target. Its interaction with biological systems and its effects on cancer cells are being studied to understand its potential as a therapeutic agent against various types of cancer.
Used in Drug Development:
2-Amino-9-(ethyl 2-carboethoxybutanoate-4-yl)purine is employed in drug development processes to identify its potential as a lead compound. Its synthesis and modification are being explored to enhance its pharmacological properties and optimize its efficacy as a therapeutic agent.
Used in Medicinal Chemistry:
In medicinal chemistry, 2-Amino-9-(ethyl 2-carboethoxybutanoate-4-yl)purine is used as a starting point for the synthesis of new compounds with potential medicinal applications. Its chemical properties and reactivity are being investigated to create novel derivatives with improved pharmacological profiles.
Note: Since the provided materials do not specify the exact applications and industries for 2-Amino-9-(ethyl 2-carboethoxybutanoate-4-yl)purine, the uses listed above are based on the general potential of such a compound in pharmaceutical and medical research. Further information would be required to provide more specific applications and industries.

Check Digit Verification of cas no

The CAS Registry Mumber 122497-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,4,9 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 122497-22:
(8*1)+(7*2)+(6*2)+(5*4)+(4*9)+(3*7)+(2*2)+(1*2)=117
117 % 10 = 7
So 122497-22-7 is a valid CAS Registry Number.

122497-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-[2-(2-aminopurin-9-yl)ethyl]propanedioate

1.2 Other means of identification

Product number -
Other names Propanedioic acid,[2-(2-amino-9H-purin-9-yl)ethyl]-,diethyl ester

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:122497-22-7 SDS

122497-22-7Relevant academic research and scientific papers

SUBSTITUTED ARYLUREA COMPOUNDS FOR INDUCING APOPTOSIS AND COMPOSITION FOR ANTICANCER COMPRISING THE SAME

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Paragraph 0130-0134, (2021/08/17)

The present invention relates to a substituted arylurea compound inducing apoptosis and an anticancer composition comprising the same. The present invention relates to a novel compound capable of preventing, treating and alleviating cancer diseases such as prostate cancer, breast cancer, lung cancer, colorectal cancer, and skin cancer by inhibiting apoptosis of cancer cells and inhibiting proliferation of cancer cells.

A direct approach to the synthesis of famciclovir and penciclovir

Choudary, Bernadette M.,Geen, Graham R.,Kincey, Peter M.,Parratt, Martin J.,Dales, J. Robert M.,Johnson, Graham P.,O'Donnell, Steven,Tudor, David W.,Woods, Neil

, p. 981 - 994 (2007/10/03)

Reaction of 2-amino-6-chloropurine with triethyl 3-bromopropane-1,1,1- tricarboxylate followed by decarbethoxylation/transsesterification of the unpurified product was the key sequence in sythesising both the anti- herpesvirus agent penciclovir and its form famciclovir in three isolated steps.

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