19549-98-5 Usage
Uses
Used in Organic Synthesis:
3,6-Dimethyl-1-heptyn-3-ol is used as an intermediate in organic synthesis for the production of other chemicals. Its unique structure allows it to be a key component in the creation of a wide range of compounds, contributing to the development of new materials and products in the chemical industry.
Used in Chemical Production:
In the chemical production industry, 3,6-Dimethyl-1-heptyn-3-ol is used as a building block for synthesizing various chemical products. Its presence in the synthesis process can lead to the creation of new compounds with specific properties, such as improved stability, reactivity, or functionality, which can be beneficial for various applications.
Used in Pharmaceutical Industry:
3,6-Dimethyl-1-heptyn-3-ol may also find applications in the pharmaceutical industry as a starting material for the synthesis of drug molecules. Its unique structure can be manipulated to create new drug candidates with potential therapeutic effects, contributing to the development of novel treatments for various medical conditions.
Used in Fragrance Industry:
In the fragrance industry, 3,6-Dimethyl-1-heptyn-3-ol can be used as a component in the creation of new scents. Its unique chemical properties may contribute to the development of innovative fragrances with distinct olfactory characteristics, enhancing the sensory experience for consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 19549-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,4 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19549-98:
(7*1)+(6*9)+(5*5)+(4*4)+(3*9)+(2*9)+(1*8)=155
155 % 10 = 5
So 19549-98-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O/c1-5-9(4,10)7-6-8(2)3/h1,8,10H,6-7H2,2-4H3/t9-/m0/s1
19549-98-5Relevant academic research and scientific papers
Regioselective Vinylation of Remote Unactivated C(sp3)?H Bonds: Access to Complex Fluoroalkylated Alkenes
Wu, Shuo,Wu, Xinxin,Wang, Dongping,Zhu, Chen
supporting information, p. 1499 - 1503 (2019/01/04)
Regioselective incorporation of a particular functional group into aliphatic sites by direct activation of unreactive C?H bonds is of great synthetic value. Despite advances in radical-mediated functionalization of C(sp3)?H bonds by a hydrogen-atom transfer process, the site-selective vinylation of remote C(sp3)?H bonds still remains underexplored. Reported herein is a new protocol for the regioselective vinylation of unactivated C(sp3)?H bonds. The remote C(sp3)?H activation is promoted by a C-centered radical instead of the commonly used N and O radicals. The reaction possesses high product diversity and synthetic efficiency, furnishing a plethora of synthetically valuable E alkenes bearing tri-/di-/mono-fluoromethyl and perfluoroalkyl groups.
Synthesis of alkyne derivatives of a novel triazolopyrazine as A 2A adenosine receptor antagonists
Yao, Gang,Haque, Serajul,Sha, Li,Kumaravel, Gnanasambandam,Wang, Joy,Engber, Thomas M.,Whalley, Eric T.,Conlon, Patrick R.,Chang, Hexi,Kiesman, William F.,Petter, Russell C.
, p. 511 - 515 (2007/10/03)
A novel [1,2,4]triazolo[1,5-a]pyrazine core was synthesized and coupled with terminal acetylenes. The structure-activity relationship of the alkynes from this novel template was studied for their in vitro and in vivo adenosine A2A receptor antagonism. Selected compounds from this series were shown to have potent in vitro and in vivo activities against adenosine A 2A receptor. Compound 12, in particular, was found to be orally active at 3 mg/kg in both a mouse catalepsy model and a 6-hydroxydopamine- lesioned rat model.
