2387-68-0 Usage
Description
(6E)-3,7,11-trimethyldodeca-6,10-dien-1-yn-3-ol, also known as a terpene alcohol, is a chemical compound with the molecular formula C15H26O. It is derived from various plant sources, such as citrus fruits and coniferous trees, and is characterized by its pleasant aroma and unique structural features, including a chain of carbon atoms and a triple bond. These properties contribute to its potential applications in different industries.
Uses
Used in Fragrance and Flavor Industry:
(6E)-3,7,11-trimethyldodeca-6,10-dien-1-yn-3-ol is used as a key component in the fragrance and flavor industry for its pleasant aroma and ability to enhance the sensory experience of various products.
Used in Antimicrobial Applications:
In the field of antimicrobial research, (6E)-3,7,11-trimethyldodeca-6,10-dien-1-yn-3-ol is used as a potential agent for its studied antimicrobial properties, which can help in the development of new treatments and products to combat microbial infections.
Used in Antioxidant Applications:
(6E)-3,7,11-trimethyldodeca-6,10-dien-1-yn-3-ol is also used as a potential antioxidant agent due to its studied antioxidant properties, which can be beneficial in various industries, such as the food and pharmaceutical industries, to enhance product shelf life and overall quality.
Used in Chemical Research and Development:
Due to its unique structure and properties, (6E)-3,7,11-trimethyldodeca-6,10-dien-1-yn-3-ol is used as a subject of study in chemical research and development for the potential discovery of new applications and the development of novel compounds with similar or enhanced properties.
Check Digit Verification of cas no
The CAS Registry Mumber 2387-68-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2387-68:
(6*2)+(5*3)+(4*8)+(3*7)+(2*6)+(1*8)=100
100 % 10 = 0
So 2387-68-0 is a valid CAS Registry Number.
2387-68-0Relevant articles and documents
Well-Defined Noble Metal Single Sites in Zeolites as an Alternative to Catalysis by Insoluble Metal Salts
Rubio-Marqués, Paula,Rivero-Crespo, Miguel A.,Leyva-Pérez, Antonio,Corma, Avelino
supporting information, p. 11832 - 11837 (2015/09/28)
Insoluble precious metal chlorides in polymeric form (i.e., PtCl2, PdCl2, AuCl, RhCl3) are commonly used as catalysts for a plethora of organic reactions in solution. Here we show that only the minor soluble fraction of these precious metal chlorides (typically 5-30%) is catalytically active for the hydroamination, hydroalkoxylation, hydrosilylation, and cycloisomerization of alkynes and alkenes, and that the resting insoluble metal is catalytically useless. To circumvent this waste of precious metal and follow a rational design, we generate here well-dispersed Pt(II) and Pd(II) single sites on zeolite Y, with an exquisite control of the Lewis acidity, to catalyze different hydroaddition reactions to alkynes and alkenes with up to 104 catalytic cycles (at least 2 orders of magnitude superior to precious metal chlorides) and with high isolated yields (82-99%, >15 examples).
SEMIHYDROGENATION OF ACETYLENES; MODIFIED LINDLAR CATALYST
Rajaram, J.,Narula, A. P. S.,Chawla, H. P. S.,Dev, Sukh
, p. 2315 - 2322 (2007/10/02)
The effect of doping Lindlar catalyst with different metal salts (shown in Table 1) on selectivity, during semihydrogenation of some acetylenes to the corresponding olefins, has been studied.Lindlar catalyst modified with MnCl2 has been found to be more selective and reproducible.
