14931-70-5 Usage
Description
1,3-diacetamido-5,7-dimethyladamantane is an organic compound characterized by its unique adamantane structure, which is a cage-like arrangement of carbon atoms. 1,3?diacetamido?5,7?dimethyladamantane features two acetamido groups at the 1 and 3 positions and two methyl groups at the 5 and 7 positions. Its structural properties make it suitable for various applications in different industries.
Uses
1. Used in the Polymer Industry:
1,3-diacetamido-5,7-dimethyladamantane is used as a monomer for the preparation of polyamides. Its unique structure contributes to the formation of strong and durable polymers with enhanced properties, such as increased thermal stability and mechanical strength.
2. Used in the Textile Industry:
In the textile industry, 1,3-diacetamido-5,7-dimethyladamantane is used as an antistatic agent for fibers and moldings. Its incorporation into the textile materials helps to reduce the buildup of static electricity, which can cause discomfort and other issues in the final product.
3. Used in the Plastics Industry:
1,3-diacetamido-5,7-dimethyladamantane can also be used in the plastics industry to improve the properties of molded products. Its addition to the polymer matrix can enhance the mechanical strength, thermal stability, and overall durability of the final product.
Check Digit Verification of cas no
The CAS Registry Mumber 14931-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,3 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14931-70:
(7*1)+(6*4)+(5*9)+(4*3)+(3*1)+(2*7)+(1*0)=105
105 % 10 = 5
So 14931-70-5 is a valid CAS Registry Number.
14931-70-5Relevant articles and documents
Synthesis of diacetylamino and diamino derivatives of adamantane series
Klimochkin, Yu. N.,Ivleva,Serzhantova,Shiryaev,Moiseev
, p. 1170 - 1175 (2017/09/29)
1,3-Diacetylamino derivatives were synthesized directly from adamantane series hydrocarbons or from adamantan-1-ylacetic acids by a one-pot method with a succession of an oxidation stage and Ritter’s reaction in nitric acid and in a mixture of sulfuric and nitric acids. The hydrolysis of 1,3-diacetylamino derivatives in an acidic medium leads to scaffold diamines and diaminoacids.
Antioxidant nitroxides and nitrones as therapeutic agents
-
, (2008/06/13)
The invention provides novel adamantane compounds having one of the following formulas: 1wherein: R1 and R3 are H, OH, alkyl, cycloalkyl, amino or aryl, and can be the same or different; R2 is H, NH2, alkyl, OH
