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1H-Purin-6-amine, N-[(3,4-dichlorophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

146579-22-8

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146579-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146579-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,5,7 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 146579-22:
(8*1)+(7*4)+(6*6)+(5*5)+(4*7)+(3*9)+(2*2)+(1*2)=158
158 % 10 = 8
So 146579-22-8 is a valid CAS Registry Number.

146579-22-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(3,4-dichlorophenyl)methyl]-7H-purin-6-amine

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:146579-22-8 SDS

146579-22-8Downstream Products

146579-22-8Relevant academic research and scientific papers

Preparation and biological activity of 6-benzylaminopurine derivatives in plants and human cancer cells

Dolezal, Karel,Popa, Igor,Krystof, Vladimir,Spichal, Lukas,Fojtikova, Martina,Holub, Jan,Lenobel, Rene,Schmuelling, Thomas,Strnad, Miroslav

, p. 875 - 884 (2007/10/03)

To study the structure-activity relationships of aromatic cytokinins, the cytokinin activity at both the receptor and cellular levels, as well as CDK inhibitory and anticancer properties of 38 6-benzylaminopurine (BAP) derivatives were compared in various

Spezific Interaction of Cytokinins and Their Analogs with Rotenone-sensitive Internal NADH Dehydrogenase in Potato Tuber Mitochondria

Sue, Masayuki,Miyoshi, Hideto,Iwamura, Hajime

, p. 1806 - 1809 (2007/10/03)

Effects of cytokinins were studied on rotenone-sensitive NADH dehydrogenase in mitochondria from fresh potato tubers (Solanum tuberosum), in consideration of the operation of external and rotenone-insensitive internal NADH dehydrogenases that has not been

Purine cytokinines in the synthesis of 2',3'-dideoxynucleosides

Hjuler-Nielsen, H. P.,Motawia, M. S.,Pedersen, E. B.,Nielsen, C.

, p. 523 - 528 (2007/10/02)

A series of 2',3'-unsaturated and 2',3'-dideoxynucleoside analogues of cytokinines have been synthesized and evaluated for their inhibitory activity against human immunodeficiency virus (HIV) in MT-4 cells. 2,3-Dideoxy sugar derivatives were coupled with the purine bases 3 according to the Friedel-Crafts catalyzed silyl Hilbert Johnson method to yield anomeric mixtures of the nucleosides 8 and 12 in 15-44percent yield.The mixtures were reacted with tetrabutylammonium fluoride (TBAF) and column chromatography separated the anomers of the desired nucleosides 9b-e, 10b-e, 13 and 14.Reverse HPLC was applied to the compounds to remove contamination by TBAF.Key Words: glycosidation / cytokinines / 2',3'-dideoxynucleosides / HIV

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