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82617-27-4

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82617-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82617-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,1 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 82617-27:
(7*8)+(6*2)+(5*6)+(4*1)+(3*7)+(2*2)+(1*7)=134
134 % 10 = 4
So 82617-27-4 is a valid CAS Registry Number.

82617-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [hydroxy-[2-[(5-methyl-2,4-dioxopyrimidin-1-yl)methoxy]ethoxy]phosphoryl] phosphono hydrogen phosphate

1.2 Other means of identification

Product number -
Other names Acyclo-TTP

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:82617-27-4 SDS

82617-27-4Downstream Products

82617-27-4Relevant articles and documents

Synthesis of acyclothymidine triphosphate and α-P-boranotriphosphate and their substrate properties with retroviral reverse transcriptase

Li, Ping,Dobrikov, Mikhail,Liu, Hongyan,Shaw, Barbara Ramsay

, p. 2401 - 2403 (2003)

(Matrix presented) The first example of an acyclonucleoside α-P-boranotriphosphate has been synthesized via a phosphoramidite approach in a one-pot reaction with good yield. The presence of the α-P-BH3 in 5b results in a 9-fold increase in efficiency of incorporation by MMLV retroviral reverse transcriptase relative to non-boronated 5a in pre-steady-state conditions. The preliminary results indicate that acyclonucleoside α-P-boranotriphosphates may have promising applications as a probe of enzyme mechanisms and in the design of new antiviral drugs.

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