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ethyl (3-methylpyridin-2-yl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41322-69-4

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41322-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41322-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,2 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41322-69:
(7*4)+(6*1)+(5*3)+(4*2)+(3*2)+(2*6)+(1*9)=84
84 % 10 = 4
So 41322-69-4 is a valid CAS Registry Number.

41322-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methyl-pyridin-2-yl)-carbamic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 3-Methyl-2-pyridyl-urethan

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:41322-69-4 SDS

41322-69-4Downstream Products

41322-69-4Relevant academic research and scientific papers

A method for synthesizing carbamate compounds by esterification reaction of amides and alcohols at room temperature

-

Paragraph 0018-0021, (2022/01/10)

The present invention discloses a method of synthesizing a carbamate compound using an esterification reaction of an amide and an alcohol at room temperature, comprising the following steps, the amide, transition metal catalyst, alcohol dissolved in an organic solvent, at room temperature, stirred for 1-6 hours, to give a mixture; filter the mixture, concentrate the filtrate, by column chromatography, to give a carbamate compound. The method of the present invention directly utilizes a common, non-toxic amide as a substrate, a wide range of substrates. The reaction takes oxygen in the air as the oxidant, the reactants do not need to be excessive, the utilization rate of raw materials is high, the substrate range is wide, the reaction conditions are mild, the operation is simple, the time is short, the yield is high, and it is suitable for application in industrial production.

Synthesis of Simple Monocyclic 1,3-Diazepines from 1,2-Diazepines

Tsuchiya, Takashi,Kurita, Jyoji,Kojima, Hirokazu

, p. 444 - 445 (2007/10/02)

Thermolysis of the 1H-1,2-diazepines having an electron-donating substituent in the 4- or 6-position affords the corresponding 1,3-diazepines, whereas 1,2-diazepines having electron-withdrawing substituents do not show this ring-conversion.

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