14433-76-2 Usage
Description
N,N-Dimethylcapramide, also known as N,N-Dimethyldecanamide, is an organic compound commonly utilized as an intermediate in the synthesis of various organic compounds. It is characterized by its amide functional group and two methyl groups attached to the nitrogen atom, which contribute to its unique chemical properties and applications.
Uses
Used in Pharmaceutical Industry:
N,N-Dimethylcapramide is used as an intermediate for the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to be a versatile building block in the development of new drugs, contributing to the advancement of medical treatments.
Used in Agrochemical Industry:
In the agrochemical industry, N,N-Dimethylcapramide is employed as an intermediate for the production of various agrochemicals. Its properties make it suitable for the synthesis of compounds used in the development of pesticides, herbicides, and other agricultural chemicals, helping to improve crop protection and yield.
Used in Veterinary Drug Industry:
N,N-Dimethylcapramide is also used as an intermediate in the veterinary drug industry. It plays a role in the synthesis of veterinary medications, contributing to the development of treatments for various animal health conditions and ensuring the well-being of livestock.
Used in Organic Synthesis:
As an intermediate for organic synthesis, N,N-Dimethylcapramide is utilized in the production of a wide range of organic compounds. Its unique structure and properties make it a valuable component in the synthesis of various chemicals used in different industries, including pharmaceuticals, agrochemicals, and others.
Check Digit Verification of cas no
The CAS Registry Mumber 14433-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,3 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14433-76:
(7*1)+(6*4)+(5*4)+(4*3)+(3*3)+(2*7)+(1*6)=92
92 % 10 = 2
So 14433-76-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H25NO/c1-4-5-6-7-8-9-10-11-12(14)13(2)3/h4-11H2,1-3H3
14433-76-2Relevant articles and documents
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Needles,H.L.,Whitfield,R.E.
, p. 989 - 990 (1966)
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Deoxygenative hydroboration of primary, secondary, and tertiary amides: Catalyst-free synthesis of various substituted amines
An, Duk Keun,Jaladi, Ashok Kumar,Kim, Hyun Tae,Yi, Jaeeun
supporting information, (2021/11/17)
Transformation of relatively less reactive functional groups under catalyst-free conditions is an interesting aspect and requires a typical protocol. Herein, we report the synthesis of various primary, secondary, and tertiary amines through hydroboration of amides using pinacolborane under catalyst-free and solvent-free conditions. The deoxygenative hydroboration of primary and secondary amides proceeded with excellent conversions. The comparatively less reactive tertiary amides were also converted to the corresponding N,N-diamines in moderate yields under catalyst-free conditions, although alcohols were obtained as a minor product.
A highly efficient catalytic α-alkylation of unactivated amides using primary alcohols
Yao, Wubing,Ma, Xiaochen,Guo, Le,Jia, Xiangqing,Hu, Aiguo,Huang, Zheng
supporting information, p. 2919 - 2921 (2016/06/13)
The α-alkylation of unactivated amides with alcohols is described. Using a NCP-type pincer Ir complex as the precatalyst and KOtBu as the base, the reactions of secondary or tertiary acetamides with benzyl or nonbenzyl primary alcohols occur at 80 °C, furnishing the alkylation products in good yields. This method represents a practical and green means of α-alkylation of amides in a relatively mild, efficient, and selective manner with low catalyst loadings (0.5 mol %).
