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74405-46-2

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  • Guanosine,5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-N-(2-methyl-1-oxopropyl)-,3'-(hydrogen butanedioate)

    Cas No: 74405-46-2

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  • 4-[[2-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-5-[2-[(2-methyl-1-oxopropyl)amino]-6-oxo-3H-purin-9-yl]-3-oxolanyl]oxy]-4-oxobutanoic acid

    Cas No: 74405-46-2

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74405-46-2 Usage

Uses

2''-Deoxy-5''-O-DMT-N2-isobutyrylguanosine 3''-O-succinate is a nucleoside used in the synthetic preparation of DNA fragments, such as small-molecule/DNA hybrids via amide coupling. 2''-Deoxy-5''-O-DMT-N2-isobutyrylguanosine 3''-O-succinate can also be used as a solid phase support for oligonucleotide synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 74405-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,0 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74405-46:
(7*7)+(6*4)+(5*4)+(4*0)+(3*5)+(2*4)+(1*6)=122
122 % 10 = 2
So 74405-46-2 is a valid CAS Registry Number.
InChI:InChI=1/C39H41N5O10/c1-23(2)36(48)42-38-41-35-34(37(49)43-38)40-22-44(35)31-20-29(54-33(47)19-18-32(45)46)30(53-31)21-52-39(24-8-6-5-7-9-24,25-10-14-27(50-3)15-11-25)26-12-16-28(51-4)17-13-26/h5-17,22-23,29-31H,18-21H2,1-4H3,(H,45,46)(H2,41,42,43,48,49)

74405-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-5-[2-(2-methylpropanoylamino)-6-oxo-3H-purin-9-yl]oxolan-3-yl]oxy-4-oxobutanoic acid

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

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More Details:74405-46-2 SDS

74405-46-2Downstream Products

74405-46-2Relevant articles and documents

Stereospecific grignard activated coupling of a deoxynucleoside: Methylphosphonate on a polyethylene glycol support

Le Bec, Christine,Wickstrom, Eric

, p. 9525 - 9528 (1994)

Stereospecific synthesis of Rp and Sp methylphosphonate diastereoisomers of d(ApG) was carried out on a polymeric support, polyethylene glycol (PEG), by the Grignard reagent solution route described by Stec. The coupling yield on PEG was higher than that observed in solution, and precipitation of the PEG at each step allowed easy separation of oligomer product from soluble reactants at each step.

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