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36226-41-2

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36226-41-2 Usage

Molecular weight

192.22 g/mol

Structure

Urea derivative with a methyl group at the 1 position and a pyridine-3-ylmethyl group at the 3 position

Potential uses

Pharmaceutical and agrochemical development, organic synthesis

Safety precautions

May pose hazards if in contact with skin, eyes, or if ingested. Proper handling and safety practices are necessary.

Check Digit Verification of cas no

The CAS Registry Mumber 36226-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,2 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36226-41:
(7*3)+(6*6)+(5*2)+(4*2)+(3*6)+(2*4)+(1*1)=102
102 % 10 = 2
So 36226-41-2 is a valid CAS Registry Number.

36226-41-2SDS

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 1-methyl-3-(pyridin-3-ylmethyl)urea

1.2 Other means of identification

Product number -
Other names 1-methyl-3-pyridin-3-ylmethyl-urea

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:36226-41-2 SDS

36226-41-2Downstream Products

36226-41-2Relevant articles and documents

Formamides as Isocyanate Surrogates: A Mechanistically Driven Approach to the Development of Atom-Efficient, Selective Catalytic Syntheses of Ureas, Carbamates, and Heterocycles

Bruffaerts, Jeffrey,Von Wolff, Niklas,Diskin-Posner, Yael,Ben-David, Yehoshoa,Milstein, David

supporting information, p. 16486 - 16493 (2019/10/14)

Despite the hazardous nature of isocyanates, they remain key building blocks in bulk and fine chemical synthesis. By surrogating them with less potent and readily available formamide precursors, we herein demonstrate an alternative, mechanistic approach to selectively access a broad range of ureas, carbamates, and heterocycles via ruthenium-based pincer complex catalyzed acceptorless dehydrogenative coupling reactions. The design of these highly atom-efficient procedures was driven by the identification and characterization of the relevant organometallic complexes, uniquely exhibiting the trapping of an isocyanate intermediate. Density functional theory (DFT) calculations further contributed to shed light on the remarkably orchestrated chain of catalytic events, involving metal-ligand cooperation.

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