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1,3,5,2,4-Trioxadisilocino7,6-bpyrrole-7(6H)-carboxylic acid, 8-(2-amino-4,5-dihydro-4-oxo-1H-pyrrolo3,2-dpyrimidin-7-yl)tetrahydro-2,2,4,4-tetrakis(1-methylethyl)-, 1,1-dimethylethyl ester, (6aR,8R,9aS)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

222854-89-9

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222854-89-9 Usage

Chemical class

Derivative of silicic acid

Contains a pyrrole-7(6H)-carboxylic acid moiety

Indicates the presence of a pyrrole ring fused with a carboxylic acid group

Tetrahydro-2,2,4,4-tetrakis(1-methylethyl) group

A saturated hydrocarbon group with four tertiary carbon atoms, each with one methyl group attached

Amino-dihydro-pyrrolo-dpyrimidin-yl component

A heterocyclic ring system containing both pyrrolo and dipyrimidinyl moieties, with an amino group attached

1,1-Dimethylethyl ester group

A tert-butyl ester group, which is a bulky and non-polar group often used to protect carboxylic acid functionalities

Pharmaceuticals

Due to its complex structure and multiple functional groups, it may have potential as a therapeutic agent or a building block for drug development

Materials science

The compound's unique structure could be utilized in the design of novel materials with specific properties

Catalysis

The presence of various functional groups may allow it to act as a catalyst or be used in the development of new catalytic systems

Check Digit Verification of cas no

The CAS Registry Mumber 222854-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,8,5 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 222854-89:
(8*2)+(7*2)+(6*2)+(5*8)+(4*5)+(3*4)+(2*8)+(1*9)=139
139 % 10 = 9
So 222854-89-9 is a valid CAS Registry Number.

222854-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3aS,9aR)-2-(2-Amino-4-oxo-4,5-dihydro-3H-pyrrolo[3,2-d]pyrimidin-7-yl)-5,5,7,7-tetraisopropyl-tetrahydro-4,6,8-trioxa-1-aza-5,7-disila-cyclopentacyclooctene-1-carboxylic acid tert-butyl ester

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:222854-89-9 SDS

222854-89-9Upstream product

222854-89-9Downstream Products

222854-89-9Relevant academic research and scientific papers

Synthesis of transition state analogue inhibitors for purine nucleoside phosphorylase and N-riboside hydrolases

Evans, Gary B.,Furneaux, Richard H.,Gainsford, Graeme J.,Schramm, Vern L.,Tyler, Peter C.

, p. 3053 - 3062 (2007/10/03)

Syntheses of the 'Immucillins', potent aza-C-nucleoside inhibitors of purine nucleoside phosphorylase are reported as well as those of 5-deoxy-, 5- deoxyfluoro- and 2-deoxy- analogues and others having modified bases. (C) 2000 Elsevier Science Ltd.

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