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560091-45-4

1-Naphthalenecarboxamide,N-2-pyrimidinyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

560091-45-4

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560091-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 560091-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,0,0,9 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 560091-45:
(8*5)+(7*6)+(6*0)+(5*0)+(4*9)+(3*1)+(2*4)+(1*5)=134
134 % 10 = 4
So 560091-45-4 is a valid CAS Registry Number.

560091-45-4SDS

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 N-(2-Pyrimidinyl)-1-naphthamide

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:560091-45-4 SDS

560091-45-4Downstream Products

560091-45-4Relevant articles and documents

Sulphuric acid immobilized on silica gel (H2SO4-SiO2) as an eco-friendly catalyst for transamidation

Rasheed,Rao, D. Nageswar,Reddy, A. Siva,Shankar, Ravi,Das, Parthasarathi

, p. 10567 - 10574 (2015/02/05)

A novel method of transamidation of carboxamides with amines by using catalytic amounts of H2SO4-SiO2 has been developed under solvent free conditions. The transamidation is compatible with a wide range of aromatic, heteroaromatic, aliphatic, cyclic/acyclic primary or secondary amines. The metal/solvent-free conditions represent a significant improvement over other existing methods as the reaction can be performed in open air conditions and no column purification is required. The versatility of this methodology was further demonstrated by synthesizing the commercially available drug procainamide.

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