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Propan-2-yl N-(4-methylpyridin-2-yl)carbamate is a chemical compound with the molecular formula C12H16N2O2. It is an organic compound that belongs to the class of carbamates, which are derivatives of carbamic acid. This specific compound features a propyl group (a three-carbon chain) attached to a nitrogen atom, which is part of a carbamate functional group. The other part of the molecule includes a 4-methylpyridin-2-yl group, indicating a pyridine ring with a methyl group at the 4-position and the nitrogen atom at the 2-position. This structure gives the compound potential applications in various fields, such as pharmaceuticals or agrochemicals, due to its ability to form strong bonds and interact with biological targets. The compound's properties, such as solubility and reactivity, can be influenced by the presence of the methyl group on the pyridine ring and the overall molecular structure.

6328-91-2

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6328-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6328-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6328-91:
(6*6)+(5*3)+(4*2)+(3*8)+(2*9)+(1*1)=102
102 % 10 = 2
So 6328-91-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2O2/c1-7(2)14-10(13)12-9-6-8(3)4-5-11-9/h4-7H,1-3H3,(H,11,12,13)

6328-91-2SDS

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 isopropyl (4-methylpyridin-2-yl)carbamate

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

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More Details:6328-91-2 SDS

6328-91-2Downstream Products

6328-91-2Relevant academic research and scientific papers

Catalyst-free synthesis of substituted pyridin-2-yl, quinolin-2-yl, and isoquinolin-1-yl carbamates from the corresponding hetaryl ureas and alcohols

Baykov, Sergey V.,Boyarskaya, Irina A.,Boyarskiy, Vadim P.,Geyl, Kirill K.,Kasatkina, Svetlana O.

, p. 6059 - 6065 (2021/07/21)

A novel catalyst-free synthesis ofN-pyridin-2-yl,N-quinolin-2-yl, andN-isoquinolin-1-yl carbamates utilizes easily accessibleN-hetaryl ureas and alcohols. The proposed environmentally friendly technique is suitable for the good-to-high yielding synthesis of a wide range ofN-pyridin-2-yl orN-quinolin-2-yl substituted carbamates featuring electron-donating and electron-withdrawing groups in the azine rings and containing various primary, secondary, and even tertiary alkyl substituents at the oxygen atom (48-94%; 31 examples). The DFT calculation and experimental study showed that the reaction proceeds through the intermediate formation of hetaryl isocyanates. The method can be applied to obtainN-isoquinolin-1-yl carbamates, although in lower yields, and ethyl benzo[h]quinolin-2-yl carbamate has also been successfully synthesized (68%).

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