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9-((2-methyl-4-methylene-5-oxotetrahydrofuran-2-yl)methyl)hypoxanthine is a complex organic compound with the molecular formula C12H12N4O3. It is a derivative of hypoxanthine, a naturally occurring purine base found in RNA, with a unique substitution at the 9-position. The compound features a 2-methyl-4-methylene-5-oxotetrahydrofuran-2-ylmethyl group attached to the hypoxanthine core, which contributes to its distinct chemical properties. This molecule is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a research tool for studying purine metabolism.

100682-44-8

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100682-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100682-44-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,8 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100682-44:
(8*1)+(7*0)+(6*0)+(5*6)+(4*8)+(3*2)+(2*4)+(1*4)=88
88 % 10 = 8
So 100682-44-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N4O3/c1-7-3-12(2,19-11(7)18)4-16-6-15-8-9(16)13-5-14-10(8)17/h5-6H,1,3-4H2,2H3,(H,13,14,17)

100682-44-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-[(2-methyl-4-methylidene-5-oxooxolan-2-yl)methyl]-3H-purin-6-one

1.2 Other means of identification

Product number -
Other names 9-Mmofh

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:100682-44-8 SDS

100682-44-8Upstream product

100682-44-8Downstream Products

100682-44-8Relevant academic research and scientific papers

Antitumor Agents. 86. Synthesis and Cytotoxicity of α-Methylene-γ-lactone-Bearing Purines

Lee, Kuo-Hsiung,Rice, Gregory K.,Hall, Iris H.,Amarnath, Venkataraman

, p. 586 - 588 (2007/10/02)

α-Methylene-γ-lactones covalently linked to adenine (3), hypoxantine (4), and guanine (5) were synthesized by using the convenient Reformatsky-type reaction between ethyl α-(bromomethyl)acrylate and the proper purine ketones.In vitro cytotoxicity data demonstrated that these compounds were active against L-1210 tissue culture cells with 3 being most potent (ED50 = 0.3 μg/mL).

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