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5'-Adenylic acid, 2'-deoxy-3'-O-[(1,1-dimethylethyl)dimethylsilyl]-, 4-nitrophenyl phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94189-85-2

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94189-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94189-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,8 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94189-85:
(7*9)+(6*4)+(5*1)+(4*8)+(3*9)+(2*8)+(1*5)=172
172 % 10 = 2
So 94189-85-2 is a valid CAS Registry Number.

94189-85-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Phosphoric acid (2R,3S,5R)-5-(6-amino-purin-9-yl)-3-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-ylmethyl ester 4-nitro-phenyl ester phenyl 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:94189-85-2 SDS

94189-85-2Relevant academic research and scientific papers

Practical Synthesis of 2'-5'-Linked Oligoadenylates (2-5A Oligomers)

Noyori, Ryoji,Uchiyama, Mamoru,Nobori, Tadahito,Hirose, Masaaki,Hayakawa, Yoshihiro

, p. 205 - 225 (2007/10/02)

A general, facile synthesis of 2'-5'-linked oligonucleotides (2-5A oligomers) has been achieved based on the second-order regioselective protection of adenosine, one-pot formation of the 2'-5' internucleotide linkage, and O-selective phosphorylation of N-unblocked nucleosides.Standard t-butyldimethylsilylation of 5'-O-p-methoxytrityladenosine followed by careful recrystallization from a mixture of triethylamine, methanol, ethyl acetate and ether (4:4:5:100 v/v) gives the 3',5'-di-O-protected adenosine in high yield.Magnesium alkoxide-mediated condensation of the 2'-O-free adenosine with o-chlorophenyl p-nitrophenyl phosphorochloridate followed by 2',3'-di-O-t-butyldimethylsilyladenosine produces the N-free and fully O-protected adenylyl(2'-5')adenosine.The resulting adenylyl dimer, after removal of the 5'-O-trityl protector, is elongated to the protected trimeric compound through a similar reaction sequence.Deprotection of the product furnishes the 2-5A core.Condensation of the 5'-O-detritylated core and bis(2,2,2-trichloroethyl) phosphorochloridate assisted by 2,6-lutidine and subsequent oxidation with aqueous iodine produces, after deblocking, 2-5A 5'-monophosphate (p5'A2'p5'pA2'p5'A).The 2-5A 5'-monophosphate is converted into 2-5A 5'-triphosphate (ppp5'A2'p5'A2'p5'A) by reaction with N,N'-carbonyldiimidazole in the presence of triethylamine followed by tributylammonium diphosphate.This procedure allows ready synthesis of 2-5A oligomers and related compounds on a multigram scale.

A CONVENIENT METHOD FOR THE FORMATION OF INTERNUCLEOTIDE LINKAGE

Hayakawa, Y.,Uchiyama, M.,Noyori, R.

, p. 4003 - 4006 (2007/10/02)

Internucleotide linkage can be made readily by reaction of N-unprotected nucleosides and phosphorochloridates or p-nitrophenyl phosphates by the assistance of Grignard reagents.

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