5877-42-9 Usage
Uses
Used in Flavor and Fragrance Industry:
4-ETHYL-1-OCTYN-3-OL is used as a flavoring agent for its sweet, floral scent, enhancing the aroma profiles in food products and beverages.
4-ETHYL-1-OCTYN-3-OL is used as a fragrance ingredient for its strong, sweet, floral odor, contributing to the creation of perfumes, soaps, and other personal care products.
Used in Pharmaceutical Industry:
4-ETHYL-1-OCTYN-3-OL is used as a synthetic intermediate in the production of pharmaceuticals, aiding in the synthesis of various medicinal compounds.
Used in Agrochemical Industry:
4-ETHYL-1-OCTYN-3-OL is used as a synthetic intermediate in the development of agrochemicals, playing a role in the creation of substances that contribute to agricultural productivity and pest control.
Used in Industrial Chemicals Production:
4-ETHYL-1-OCTYN-3-OL is used as a synthetic intermediate for the production of other industrial chemicals, facilitating the creation of a range of chemical products used across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5877-42-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5877-42:
(6*5)+(5*8)+(4*7)+(3*7)+(2*4)+(1*2)=129
129 % 10 = 9
So 5877-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-4-7-8-9(5-2)10(11)6-3/h3,9-11H,4-5,7-8H2,1-2H3
5877-42-9Relevant academic research and scientific papers
Synthesis of acetylenic alcohols with calcium carbide as the acetylene source
Sum, Yin Ngai,Yu, Dingyi,Zhang, Yugen
supporting information, p. 2718 - 2721 (2013/10/08)
Propargyl alcohols containing a terminal alkyne group are highly important and versatile intermediates. Here, we report the synthesis of these compounds from an inexpensive and renewable resource, calcium carbide (CaC2). No metal catalysts are required in this new protocol and the reactions take place under very mild conditions.
METHOD FOR PRODUCING A PROPARGYL ALCOHOL AND AN ALLYL ALCOHOL
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Page/Page column 8, (2008/06/13)
The invention relates to a method for producing a propargyl alcohol of formula (I) wherein R1 represents a C1-30 alkyl radical, a C3-8 cycloalkyl radical, a C2-20 alkoxyalkyl radical, a C6-14 aryl radical, a C7-20 alkoxyaryl radical, a C7-20 aralkyl radical, a C7-20 alkylaryl radical or H. According to said method, a corresponding aldehyde of formula R1-CHO is reacted with acetylene in the presence of ammonia and a catalytic quantity of between 0.6 and 10 mol % of an alkaline metal hydroxide, an alkaline earth metal hydroxide or an alkaline metal alcoholate, in relation to the aldehyde used. The invention also relates to a method for producing an allyl alcohol of formulae (II) and (III), from the propargyl alcohol (I) produced according to the invention.
