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BIS(TRIMETHYLSILYL)HYPOXATHINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17962-89-9

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17962-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17962-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,6 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17962-89:
(7*1)+(6*7)+(5*9)+(4*6)+(3*2)+(2*8)+(1*9)=149
149 % 10 = 9
So 17962-89-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H20N4OSi2/c1-17(2,3)15-8-14-9-10(15)12-7-13-11(9)16-18(4,5)6/h7-8H,1-6H3

17962-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name BIS(TRIMETHYLSILYL)HYPOXATHINE

1.2 Other means of identification

Product number -
Other names 6-(Trimethylsiloxy)-9-(trimethylsilyl)-9H-purine

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:17962-89-9 SDS

17962-89-9Relevant academic research and scientific papers

ANALOGS OF PURINE NUCLEOSIDES. 3. ALKOXYALKYLATION OF HYPOXANTHINE BY THE SILYL METHOD

Madre, M.A.,Liepin'sh, E.E.,Zhuk, R.A.,Sakhartova, O.V.,Lidak, M.Yu.

, p. 425 - 431 (1986)

The reaction of bis(trimethylsilyl)hypoxanthine with methyl trichloromethyl ether has been investigated. 1-Methoxymethyl-, 7-methoxymethyl, and 9-methoxymethylhypoxanthine, as well as 1,7-, 1,9-, and 3,7-bismethoxymethylhypoxanthine, have been isolated fr

Chitosan–silica sulfate nanohybrid: a highly efficient and green heterogeneous nanocatalyst for the regioselective synthesis of N-alkyl purine, pyrimidine and related N-heterocycles via presilylated method

Behrouz, Somayeh,Soltani Rad, Mohammad Navid,Piltan, Mohammad Amin

, p. 113 - 124 (2019/07/30)

Abstract: The presilylation of purine and pyrimidine nucleobases as well as other related N-heterocycles with HMDS utilizing chitosan–silica sulfate nanohybrid (CSSNH) is described. CSSNH is proved to be a useful, highly efficient and eco-friendly heterogeneous nanohybrid catalyst for silylation of nucleobases. The presilylated nucleobases then underwent the reaction with different sources of carbon electrophiles to afford the desired N-alkyl-substituted derivatives in good-to-excellent yields. CSSNH exhibits several advantageous involving ease of handling and preparation, low cost, reusability and environmental benignity. These unique properties render the CSSNH to be an ideal candidate for use in green industrial processes. Graphic abstract: [Figure not available: see fulltext.].

Silica sulfuric acid (SSA) as a highly efficient heterogeneous catalyst for persilylation of purine and pyrimidine nucleobases and other N-heterocycles using HMDS

Rad, Mohammad Navid Soltani,Khalafi-Nezhad, Ali,Divar, Masoumeh,Behrouz, Somayeh

experimental part, p. 1943 - 1954 (2010/11/16)

Purine and pyrimidine nucleobases and other N-heterocycles have been silylated with HMDS in excellent yields in the presence of a catalytic amount of silica sulfuric acid (SSA) as a heterogeneous catalyst. SSA utilizes a shorter reaction time and higher yields of silylated nucleobases. SSA is reusable for several times without a decrease in reactivity or yield of silylated adducts. Copyright

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