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1-(6-amino-9H-purin-9-yl)-3-(prop-2-en-1-yloxy)propan-2-ol is a chemical compound that features a purine molecule with a six-membered ring composed of four nitrogen atoms and two carbon atoms. 1-(6-amino-9H-purin-9-yl)-3-(prop-2-en-1-yloxy)propan-2-ol also includes a propanol group, which is made up of three carbon atoms and a hydroxyl group. Furthermore, it has a propen-1-yloxy group connected to the propanol group, characterized by a double bond between two carbon atoms and an oxygen atom. Structurally related to nucleotides and nucleosides, which play a crucial role in DNA and RNA synthesis, 1-(6-amino-9H-purin-9-yl)-3-(prop-2-en-1-yloxy)propan-2-ol may hold potential applications in the fields of pharmaceuticals and biochemistry due to its unique structural properties.

89760-74-7

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89760-74-7 Usage

Uses

Used in Pharmaceutical Industry:
1-(6-amino-9H-purin-9-yl)-3-(prop-2-en-1-yloxy)propan-2-ol is used as a potential therapeutic agent for [application reason] due to its structural resemblance to nucleotides and nucleosides, which are essential in DNA and RNA synthesis.
Used in Biochemical Research:
In the field of biochemistry, 1-(6-amino-9H-purin-9-yl)-3-(prop-2-en-1-yloxy)propan-2-ol serves as a valuable compound for [application reason], possibly contributing to the understanding of nucleotide and nucleoside interactions and their roles in cellular processes.

Check Digit Verification of cas no

The CAS Registry Mumber 89760-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,6 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89760-74:
(7*8)+(6*9)+(5*7)+(4*6)+(3*0)+(2*7)+(1*4)=187
187 % 10 = 7
So 89760-74-7 is a valid CAS Registry Number.

89760-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-aminopurin-9-yl)-3-prop-2-enoxypropan-2-ol

1.2 Other means of identification

Product number -
Other names 9-<2-hydroxy-3-allyloxy-propyl>adenine

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:89760-74-7 SDS

89760-74-7Downstream Products

89760-74-7Relevant academic research and scientific papers

Synthesis of unsaturated adenine derivatives, potential inhibitors of S-adenosyl-L-homocysteine hydrolase

Ozerov,Novikov

, p. 712 - 715 (1996)

The synthesis of 9-substituted adenine derivatives, containing an unsaturated fragment at the end of the acyclic chain, is described; it consists of the alkylation of adenine salts with unsaturated α-haloethers, tosylates, and epoxides. It was shown that compounds of this series possess moderate antiviral activity. 1997 Plenum Publishing Corporation.

Synthesis and hypolipemic activity of new 9-substituted adenines

Roveri,Cavrini,Gatti,et al.

, p. 555 - 557 (2007/10/02)

9-[2-(2,3-Dihydroxypropyloxy)ethyl] adenine 2 and 9-[2-hydroxy-3-(2,3-dihydroxypropyloxy)propyl] adenine 3 were synthesized and tested for their hyperlipemic activities in rats. Compound 2 showed a significant cholesterol-lowering effect while 3 reduced t

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