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Carbamic acid, dimethyl-, pentyl ester, also known as dimethylcarbamic acid pentyl ester, is an organic compound with the chemical formula C8H17NO2. It is a derivative of carbamic acid, where two methyl groups and a pentyl group are attached to the carbamic acid molecule. This ester is a colorless liquid with a mild, fruity odor and is soluble in most organic solvents. It is primarily used as a synthetic intermediate in the production of various agrochemicals, pharmaceuticals, and other chemical compounds. Due to its potential applications in the synthesis of pesticides and other chemicals, it is essential to handle Carbamic acid, dimethyl-, pentyl ester with care, as it may have toxic effects on humans and the environment.

2594-36-7

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2594-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2594-36-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2594-36:
(6*2)+(5*5)+(4*9)+(3*4)+(2*3)+(1*6)=97
97 % 10 = 7
So 2594-36-7 is a valid CAS Registry Number.

2594-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name pentyl N,N-dimethylcarbamate

1.2 Other means of identification

Product number -
Other names amyl dimethylcarbamate

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:2594-36-7 SDS

2594-36-7Downstream Products

2594-36-7Relevant academic research and scientific papers

FREE-RADICAL REACTIONS OF N,N-DIMETHYLAMINODIALKOXYMETHANES

Kurbanov, D.,Pastushenko, E. V.,Zlot-skii, S. S.,Rakhmankulov, D. L.

, p. 850 - 854 (2007/10/02)

The homolytic liquid-phase reactions of N,N-dimethylaminodialkoxymethanes, initiated by tert-butoxyl radicals in the range of 120-150 deg C, were investigated.The mechanism of the unbranched chain process of fragmentation of the acetals with quadratic chain termination at the alkyl radicals was determined.As a result the corresponding dimethylcarbamic esters, dimethylformamide, alkanes, and carbonyl compounds were formed.The relative rate constants for the transformations of the nitrogen analogs of the ortho esters were calculated.The difference in the activation energies for the cleavage of the C-H bonds adjacent to one and three heteroatoms was determined for N,N-dimethylaminodimethoxymethane (ΔE=5 kcal/mole) and N,N-dimethylaminodipentyloxymethane (ΔE=8 kcal/mole).

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