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Adenosine, 2'-azido-N-benzoyl-2',3'-dideoxy-3'-fluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

195304-70-2

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195304-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 195304-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,3,0 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 195304-70:
(8*1)+(7*9)+(6*5)+(5*3)+(4*0)+(3*4)+(2*7)+(1*0)=142
142 % 10 = 2
So 195304-70-2 is a valid CAS Registry Number.

195304-70-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[9-[(2R,3S,4S,5R)-3-azido-4-fluoro-5-(hydroxymethyl)oxolan-2-yl]purin-6-yl]benzamide

1.2 Other means of identification

Product number -
Other names Adenosine,2'-azido-N-benzoyl-2',3'-dideoxy-3'-fluoro

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:195304-70-2 SDS

195304-70-2Relevant academic research and scientific papers

Synthesis and biological activity of modified (2'-5')triadenylates containing 2'-terminal 2',3'-dideoxy-3'-fluoroadenosine derivatives

Kvasyuk,Kulak,Tkachenko,Sentyureva,Mikhailopulo,Suhadolnik,Heoderson,Horvath,Guan,Pfleiderer

, p. 1278 - 1284 (2007/10/03)

Some new (2'-5')triadenylates 13-16, containing at the 2'-terminal end 3'-fluoro-2',3'-dideoxyadenosine derivatives, have been synthesized by the phosphotriester method. The selectively blocked nucleosides 2, 4, 5, and 7 were synthesized from the corresponding unprotected 'nucleosides 1, 3, and 6. The synthesized trimers 13 and 14 were 4- and 8-fold, respectively, more stable towards phosphodiesterase from Crotalus durissus than the natural trimer 17. In comparison to trimer 17 the new compounds 13-15 inhibit HIV-1 reverse transcriptase (RT) activity, and 15 and 16 the HIV-1 induced syncytia formation 2-3 fold whereas none of 13-16 can improve RNase L activity.

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