41319-54-4 Usage
Uses
Used in Organic Synthesis:
N,N-dioctadecylcarbamoyl chloride is used as a reagent for forming stable amide linkages with amines and other nucleophiles, which is crucial in the preparation of amides and other important organic compounds. Its ability to create these linkages contributes to its utility in various chemical reactions and the synthesis of a wide range of organic products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N,N-dioctadecylcarbamoyl chloride is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its role in creating stable amide bonds is essential for the development of new drugs and the modification of existing ones to enhance their efficacy and stability.
Used in Chemical Research:
N,N-dioctadecylcarbamoyl chloride is also employed in chemical research for studying the properties of amide bonds and the reactions involving nucleophiles. Its use in research helps to advance the understanding of organic chemistry and contributes to the discovery of new chemical reactions and compounds.
Safety Precautions:
Due to its corrosive nature, N,N-dioctadecylcarbamoyl chloride should be handled with care in a well-ventilated area, and appropriate safety measures, including the use of personal protective equipment, should be taken to minimize the risk of inhalation or ingestion.
Check Digit Verification of cas no
The CAS Registry Mumber 41319-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,1 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41319-54:
(7*4)+(6*1)+(5*3)+(4*1)+(3*9)+(2*5)+(1*4)=94
94 % 10 = 4
So 41319-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C37H74ClNO/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-39(37(38)40)36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-36H2,1-2H3
41319-54-4Relevant academic research and scientific papers
"Solvent Friction" and the Entanglement of Long Hydrocarbon Chains
Menger, F. M.,Mounier, C. E.
, p. 1655 - 1656 (2007/10/02)
Rotation about the R2N-COOR bond in carbamates with three alkyl chains (butyl through octadecyl) was investigated by NMR.Even solvents such as hexadecane and mineral oil did not substantially impede the rotation, revealing a surprising absence of "solvent friction" induced by chain entanglement.Possible explanations at the molecular level and the relevance to membrane systems are discussed.
Xylene-diamines as antiviral agents
-
, (2008/06/13)
Compounds of the formula STR1 or a non-toxic acid addition salt thereof wherein R1 is alkyl of from 1 to 20 carbon atoms; R2 is alkyl of from 12 to 20 carbon atoms; R3 is selected from the group consisting of hydrogen and hydroxyalkyl of from 2 to 8 carbon atoms; and R4 is selected from the group consisting of hydrogen, alkyl of from 1 to 8 carbon atoms and hydroxyalkyl of from 2 to 8 carbon atoms, said compounds are useful for combating viral infections in vertebrate animals.
