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6456-92-4

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6456-92-4 Usage

General Description

2(1H)-Pyridinone, 1,3-dimethyl-, also known as 3,5-lutidine, is a chemical compound with the molecular formula C7H9N and a molecular weight of 107.15 g/mol. It is a clear, colorless liquid with a pungent, ammonia-like odor. It is commonly used as a solvent and intermediate in the production of pharmaceuticals, dyes, rubber chemicals, and pesticides. It is also used as a building block in the synthesis of agrochemicals and pharmaceuticals. 3,5-lutidine is considered to be a hazardous substance and should be handled with care due to its potential to cause irritation to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 6456-92-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,5 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6456-92:
(6*6)+(5*4)+(4*5)+(3*6)+(2*9)+(1*2)=114
114 % 10 = 4
So 6456-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO/c1-6-4-3-5-8(2)7(6)9/h3-5H,1-2H3

6456-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2(1H)-Pyridinone, 1,3-dimethyl-

1.2 Other means of identification

Product number -
Other names 1,3-dimethyl-1H-pyridin-2-one

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:6456-92-4 SDS

6456-92-4Relevant articles and documents

Toluene and its Derivatives as Atom-Efficient Benzylating Agents for Secondary Amines

Sch?nbauer, David,Lukas, Florian,Schnürch, Michael

supporting information, p. 94 - 98 (2019/01/04)

Toluene as a replacement for common N -benzylating agents, such as benzyl bromide, can be an atom-efficient alternative reagent. Under nickel catalysis and mildly oxidative conditions, it is possible to activate toluene efficiently and use it directly for the benzylation of different 2-aminopyridines. The transformation is not restricted to simple toluene, but also substituted derivatives give the desired product in good yields. Effective cleavage of the pyridine moiety is presented.

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