19780-39-3 Usage
Uses
Used in the Solvent Industry:
3-Ethyl-2-heptanol is used as a solvent for its ability to dissolve a wide range of substances, making it a valuable component in the formulation of various products.
Used in Perfumery and Flavoring Industry:
3-Ethyl-2-heptanol is used as a fragrance and flavoring agent, capitalizing on its pleasant fruity scent to enhance the aroma and taste of consumer products.
Used as a Chemical Intermediate:
In the chemical industry, 3-Ethyl-2-heptanol serves as an intermediate in the synthesis of other organic compounds, contributing to the creation of a diverse array of chemical products.
Used in Pharmaceutical Manufacturing:
3-Ethyl-2-heptanol is utilized in the production of pharmaceuticals, playing a crucial role in the development of medications and other healthcare-related products.
Used in Industrial Applications:
Beyond its uses in specific industries, 3-Ethyl-2-heptanol is also employed in various industrial applications, showcasing its adaptability and broad utility in different settings.
While 3-Ethyl-2-heptanol is considered relatively non-toxic, it is important to note that prolonged or repeated exposure may lead to irritation of the skin, eyes, and respiratory system, highlighting the need for proper handling and safety measures during its use.
Check Digit Verification of cas no
The CAS Registry Mumber 19780-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,8 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19780-39:
(7*1)+(6*9)+(5*7)+(4*8)+(3*0)+(2*3)+(1*9)=143
143 % 10 = 3
So 19780-39-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O/c1-4-6-7-9(5-2)8(3)10/h8-10H,4-7H2,1-3H3/t8-,9+/m1/s1
19780-39-3Relevant academic research and scientific papers
Pheromone Synthesis, CLIV. Synthesis of the Stereoisomers of 3-Methyl-4-octanol to Determine the Absolute Configuration of the Naturally Occuring (3S,4S)-Isomer Isolated as the Male-Produced Aggregation Pheromone of the African Palm Weevil, Rhynchophorus
Mori, Kenji,Kiyota, Hiromasa,Rochat, Didier
, p. 865 - 870 (2007/10/02)
The relative configuration of the naturally occuring 3-methyl-4-octanol (1), the male-produced aggregation pheromone of Rhynchophorus phoenicis, was determined as syn by a GC comparison of the synthetic (+/-)-syn- and (+/-)-anti-1 with the natural product
