Welcome to LookChem.com Sign In|Join Free

CAS

  • or

25589-18-8

Post Buying Request

25589-18-8 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

25589-18-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25589-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,8 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25589-18:
(7*2)+(6*5)+(5*5)+(4*8)+(3*9)+(2*1)+(1*8)=138
138 % 10 = 8
So 25589-18-8 is a valid CAS Registry Number.

25589-18-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzyl-6-methyl-1H-pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-Benzyl-6-methyl-1H-pyrimidin-2,4-dion

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:25589-18-8 SDS

25589-18-8Relevant articles and documents

Direct Chemoselective Synthesis of N-3-Substituted Pyrimidinones in a Microwave-Assisted Method

Laxminarayana, Burgula,Kundu, Lal Mohan

supporting information, p. 1342 - 1353 (2015/05/26)

Synthesis of selectively N-3-substituted pyrimidine nucleobases or pyrimidinones has always been a challenge because of poor regioselectivity and chemoselectivity. In this article we demonstrate a single-step, de novo synthesis of selectively N-3-substitu

Heterocyclic Transformations. Part 6. Studies on the Reactions of 3-Benzyl-6-methyl-1,3-oxazine-2,4(3H)-dione with α-Amino and Hydroxy Amides

Singh, Harjit,Singh, Palwinder,Chimni, Swapandeep Singh,Kumar, Subodh

, p. 364 - 365 (2007/10/03)

Amide nitrogen-induced reactions of α-amino and hydroxy amides with 3-benzyl-6-methyl-1,3-oxazine-2,4(3H)-dione 1 give 6-substituted-5-acetyluracils 2; a competitive reaction initiated by the amine nitrogen of an amino amide in some cases also yields 1-su

A useful methodology for the regioselective deprotection of 1,3-dibenzyluracils

Botta,Summa,Saladino,Nicoletti

, p. 2181 - 2187 (2007/10/02)

A practical, regioselective N-1 deprotection of 1,3-dibenzyl uracils 2 a-e is described. The same experimental procedure and longer reaction time afforded the complete deprotection of the uracils.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 25589-18-8