17678-60-3 Usage
General Description
N,N-dimethylpentadecylamine is an organic chemical compound belonging to the amine class of chemicals. It consists of a pentadecyl chain, which is a long hydrocarbon chain with 15 carbon atoms, and two methyl groups attached to a nitrogen atom. N,N-dimethylpentadecylamine is commonly used as a surfactant and emulsifier in various industrial applications, such as in the production of personal care products, pharmaceuticals, and lubricants. It is also used in the synthesis of other chemical compounds and as a corrosion inhibitor. N,N-dimethylpentadecylamine is known for its ability to lower the surface tension of liquids and facilitate the mixing of substances that are typically immiscible. It is important to handle this chemical with care, as it can be harmful if inhaled, ingested, or comes into contact with the skin or eyes.
Check Digit Verification of cas no
The CAS Registry Mumber 17678-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,7 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17678-60:
(7*1)+(6*7)+(5*6)+(4*7)+(3*8)+(2*6)+(1*0)=143
143 % 10 = 3
So 17678-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H37N/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(2)3/h4-17H2,1-3H3
17678-60-3Relevant articles and documents
Methylformate as replacement of syngas in one-pot catalytic synthesis of amines from olefins
Karakhanov, Eduard,Maksimov, Anton,Kardasheva, Yulia,Runova, Elena,Zakharov, Roman,Terenina, Maria,Kenneally, Corey,Arredondo, Victor
, p. 540 - 547 (2014/02/14)
A new general approach for the one-pot hydroaminomethylation of olefins using methylformate as formylating agent instead of synthesis gas (syngas) has been proposed. Herein we report that a Ru-Rh catalytic system demonstrates high activity in a tandem conversion of a series of n-alkenes into amines using methylformate with yields 58-92% (6 h). The selectivity for the normal amine reached 96% with catalysis by the Ru carbonyl complex Ru3(CO) 12, with an overall yield of 55% with respect to amine in this instance. The addition of the Rh complex to Ru catalytic system, sharply increased the hydroaminomethylation rate of both the terminal and internal alkenes and increased the yield of amines to 82-93% (6-12 h). The Royal Society of Chemistry.
