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5-[hydroxy(phenyl)methyl]pyrimidine-2,4(1H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92016-66-5

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92016-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92016-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,1 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92016-66:
(7*9)+(6*2)+(5*0)+(4*1)+(3*6)+(2*6)+(1*6)=115
115 % 10 = 5
So 92016-66-5 is a valid CAS Registry Number.

92016-66-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[hydroxy(phenyl)methyl]-1H-pyrimidine-2,4-dione

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:92016-66-5 SDS

92016-66-5Downstream Products

92016-66-5Relevant 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

Grignard and cerium reagents of pyrimidine derivatives

Shimura, Akihiko,Momotake, Atsuya,Togo, Hideo,Yokoyama, Masataka

, p. 495 - 499 (2007/10/03)

5-(Pyrimidinyl)magnesium and cerium chlorides were prepared via the halogen-metal exchange of 5-bromopyrimidine with ethylmagnesium chloride and a sequential treatment of butyl-lithium and cerium(III) chloride, respectively. In a similar way, 5-[2,4-di(te

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