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7-(6-amino-9H-purin-9-yl)heptanoic acid, also known as 7-(6-aminopurine-9-yl)heptanoic acid, is a chemical compound with the molecular formula C12H17N5O2. It is a derivative of purine, a heterocyclic aromatic organic compound consisting of a pyrimidine ring fused to an imidazole ring. 7-(6-amino-9H-purin-9-yl)heptanoic acid is characterized by the presence of an amino group attached to the purine ring and a heptanoic acid chain. It is a white crystalline solid and is soluble in water. The compound has potential applications in the pharmaceutical industry, particularly in the synthesis of nucleoside analogs, which are used as antiviral and anticancer agents. Its chemical structure and properties make it a valuable intermediate in the development of new therapeutic agents.

4323-13-1

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4323-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4323-13-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,2 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4323-13:
(6*4)+(5*3)+(4*2)+(3*3)+(2*1)+(1*3)=61
61 % 10 = 1
So 4323-13-1 is a valid CAS Registry Number.

4323-13-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-(6-aminopurin-9-yl)heptanoic acid

1.2 Other means of identification

Product number -
Other names 6-Amino-9H-purinyl-heptansaeure

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:4323-13-1 SDS

4323-13-1Downstream Products

4323-13-1Relevant academic research and scientific papers

Regulation of type 5 adenylyl cyclase for treatment of neurodegenerative and cardiac diseases

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Page/Page column 29, (2010/11/24)

The invention concerns pharmaceutical compositions that contain a compound or compounds that can effectively regulate the activity of Type 5 Adenylyl Cyclase and methods for treatment of neurological diseases and disorders, as well as motor function loss

Hydroxamate based inhibitors of adenylyl cyclase. Part 1: The effect of acyclic linkers on P-site binding

Levy, Daniel E,Marlowe, Charles,Kane-Maguire, Kim,Bao, Ming,Cherbavaz, Diana B.,Tomlinson, James E.,Sedlock, David M.,Scarborough, Robert M.

, p. 3085 - 3088 (2007/10/03)

The adenylyl cyclases (ACs) are a family of enzymes that are key elements of signal transduction by virtue of their ability to convert ATP to cAMP. The catalytic mechanism of this transformation proceeds through initial binding of ATP to the purine bindin

Polymethylene Derivatives of Nucleic Bases with ω-Functional Groups: II. Adenine and Hypoxanthine Derivatives

Makinsky,Kritzyn,Ul'yanova,Zakharova,Bugreev,Nevinsky

, p. 167 - 172 (2007/10/03)

N9-Polymethylene derivatives of adenine and hypoxanthine with various functional groups in the ω-position of the alkyl substituent were synthesized. Their physicochemical properties and effect on the HIV reverse transcriptase and DNA topoisomerase I were studied.

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