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5-(Trimethylsilyl)uracil is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59523-07-8

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59523-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59523-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,2 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59523-07:
(7*5)+(6*9)+(5*5)+(4*2)+(3*3)+(2*0)+(1*7)=138
138 % 10 = 8
So 59523-07-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2O2Si/c1-12(2,3)5-4-8-7(11)9-6(5)10/h4H,1-3H3,(H2,8,9,10,11)

59523-07-8SDS

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 5-trimethylsilyl-1H-pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-trimethylsilyluracil

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:59523-07-8 SDS

59523-07-8Downstream Products

59523-07-8Relevant academic research and scientific papers

Functionalization of unprotected uracil derivatives using the halogen - Magnesium exchange

Kopp, Felix,Knoechel, Paul

, p. 1639 - 1641 (2008/02/02)

The reaction of commercially available 5-iodouracil with 2 equiv of MeMgCl in the presence of LiCl, followed by the addition of i-PrMgCl-LiCl, provides the corresponding trimagnesiated species, which reacts with various electrophiles to give selectively 5

Preparation of allyl-, alkenyl- and of functionalized arylmanganese reagents by oxidative insertion of manganese-graphite into organic halides

Fuerstner, Alois,Brunner, Heiko

, p. 7009 - 7012 (2007/10/03)

Reduction of MnBr2·nLiBr (n = 1,2) with 2 C8K in THF affords highly active Mn-graphite, which readily insert into allyl-, alkenyl-, (substituted) aryl- and heteroaryl halides. The functionalized organomanganese compounds thus obtained may be efficiently trapped with different electrophiles such as aldehydes, anhydrides and acid chlorides, or can be cross-coupled with alkenyl halides in the presence of catalytic amounts of Fe(acac)3.

Synthesis of silyl and stannyl pyrimidines

Parkanyi, Cyril,Cho, Nam Sook,Yoo, Geon Seek

, p. 1 - 8 (2007/10/02)

2,4-dimethoxy- and 2,4-dibenzyloxy-5-lithiopyrimidines, obtained from the corresponding substituted 5-bromopyrimidines, react with trimethylsilyl chloride or trimethylstannyl chloride to give the appropriate 5-trimethylsilyl or trimethylstannyl derivative

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