67952-46-9 Usage
Description
2-(1-methylethoxy)ethyl carbamate is a carbamate ester with the molecular formula C7H15NO3. It is a versatile chemical compound commonly used as a solvent and a chemical intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds.
Uses
Used in Pharmaceutical Industry:
2-(1-methylethoxy)ethyl carbamate is used as a chemical intermediate for the synthesis of various pharmaceutical drugs, including sedatives, anesthetics, and muscle relaxants. Its properties make it a valuable component in the development of these medications.
Used in Agrochemical Industry:
2-(1-methylethoxy)ethyl carbamate is used in the formulation of insecticides and herbicides. Its ability to act as a solvent and chemical intermediate contributes to the effectiveness of these products in controlling pests and unwanted plant growth.
Used in Polymer and Resin Production:
2-(1-methylethoxy)ethyl carbamate is used as a stabilizer and plasticizer in the production of polymers and resins. Its incorporation into these materials enhances their stability and flexibility, making them suitable for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 67952-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,5 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67952-46:
(7*6)+(6*7)+(5*9)+(4*5)+(3*2)+(2*4)+(1*6)=169
169 % 10 = 9
So 67952-46-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO3/c1-5(2)9-3-4-10-6(7)8/h5H,3-4H2,1-2H3,(H2,7,8)
67952-46-9Relevant articles and documents
Silica supported perchloric acid (HClO4-SiO2): an efficient reagent for the preparation of primary carbamates under solvent-free conditions
Modarresi-Alam, Ali Reza,Khamooshi, Ferydoon,Nasrollahzadeh, Mahmoud,Amirazizi, Homeyra Alsadat
, p. 8723 - 8726 (2008/02/11)
The synthesis of primary carbamates from structurally diverse compounds containing a hydroxyl group has been performed in high yields and purity, and without any epimerization under solvent-free conditions using HClO4-SiO2 as a mild, convenient, and effective reagent. The procedure is operationally simple, efficient, and environmentally benign.
