2114-20-7 Usage
General Description
Carbamic acid hexyl ester is a chemical compound that belongs to the family of carbamates. It has the molecular formula C7H15NO2. Carbamates are organic compounds derived from carbamic acid (NH2COOH) and are often used in the production of pesticides, fungicides, herbicides, and pharmaceuticals. As far as specific uses or applications of carbamic acid hexyl ester, information is limited. However, like other carbamates, it may also potentially be used in similar roles or functions. Its properties and potential hazards should be handled and evaluated with care just like any other chemical substances. As always, proper safety protocols should be followed when handling any chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 2114-20-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2114-20:
(6*2)+(5*1)+(4*1)+(3*4)+(2*2)+(1*0)=37
37 % 10 = 7
So 2114-20-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO2/c1-2-3-4-5-6-10-7(8)9/h2-6H2,1H3,(H2,8,9)
2114-20-7Relevant articles and documents
Indium(III)-Catalyzed Synthesis of Primary Carbamates and N-Substituted Ureas
Jain, Isha,Malik, Payal
supporting information, p. 93 - 97 (2021/11/26)
An indium triflate-catalyzed synthesis of primary carbamates from alcohols and urea as an ecofriendly carbonyl source has been developed. Various linear, branched, and cyclic alcohols were converted into the corresponding carbamates in good to excellent yields. This method also provided access to N-substituted ureas by carbamoylation of amines. All the products were obtained by simple filtration or crystallization, without the need for chromatographic purification. Mechanistic investigations suggest that the carbamoylation reaction proceeds through activation of urea by O-coordination with indium, followed by nucleophilic attack by the alcohol or amine on the carbonyl center of urea. The inexpensive and easily available starting materials and catalyst, the short reaction times, and the ease of product isolation highlight the inherent practicality of the developed method.
