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66341-18-2

66341-18-2

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  • 2-[(2-amino-6-oxo-3H-purin-9-yl)methoxy]ethyl[hydroxy(phosphonooxy)phosphoryl] hydrogen phosphate

    Cas No: 66341-18-2

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66341-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66341-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,4 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66341-18:
(7*6)+(6*6)+(5*3)+(4*4)+(3*1)+(2*1)+(1*8)=122
122 % 10 = 2
So 66341-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H11N5O3.3H3O4P/c9-8-11-6-5(7(15)12-8)10-3-13(6)4-16-2-1-14;3*1-5(2,3)4/h3,14H,1-2,4H2,(H3,9,11,12,15);3*(H3,1,2,3,4)

66341-18-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[(2-amino-6-oxo-3H-purin-9-yl)methoxy]ethoxy-hydroxyphosphoryl] phosphono hydrogen phosphate

1.2 Other means of identification

Product number -
Other names Aciclovir-triphosphate

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:66341-18-2 SDS

66341-18-2Downstream Products

66341-18-2Relevant articles and documents

Engineering a selective small-molecule substrate binding site into a deoxyribozyme

Hoebartner, Claudia,Silverman, Scott K.

, p. 7420 - 7424 (2007)

A small goal: An RNA ligase deoxyribozyme is engineered to accept a small-molecule NTP substrate in a multiple-turnover fashion. Selective binding is enforced by hydrogen bonding, and structural preorganization within the NTP itself is important for its efficient utilization as a substrate. This study points the way toward a broader use of small-molecule substrates with nucleic acid enzymes. (Figure Presented)

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