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Acetamide, N-[9-(2-oxopropyl)-9H-purin-6-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105970-01-2

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105970-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105970-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,7 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105970-01:
(8*1)+(7*0)+(6*5)+(5*9)+(4*7)+(3*0)+(2*0)+(1*1)=112
112 % 10 = 2
So 105970-01-2 is a valid CAS Registry Number.

105970-01-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[9-(2-oxopropyl)purin-6-yl]acetamide

1.2 Other means of identification

Product number -
Other names -

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:105970-01-2 SDS

105970-01-2Relevant academic research and scientific papers

Regioselective N9 alkylation of purine rings assisted by β-cyclodextrin

Zhang, Qian,Cheng, Gang,Huang, Yong-Zhen,Qu, Gui-Rong,Niu, Hong-Ying,Guo, Hai-Ming

experimental part, p. 7822 - 7826 (2012/09/22)

Under the assistance of β-cyclodextrin, purine was effectively alkylated at N9 together with up to 99% conversion and good to excellent yield using water as the solvent. High regioselectivity-N9/N7 selectivity>99:1 was attributed to the β-cyclodextrin cav

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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