100189-17-1 Usage
Description
6-Methyl-3-pyridineethanol, also known as 3-(2-Hydroxyethyl)pyridine, is an organic compound with a chemical structure that features a pyridine ring with a methyl group at the 6th position and an ethanol group at the 3rd position. It is a yellow solid and is commonly used as a reactant in organic synthesis due to its unique chemical properties.
Uses
Used in Organic Synthesis:
6-Methyl-3-pyridineethanol is used as a reactant in organic synthesis for the production of various chemical compounds. Its unique structure allows it to participate in a wide range of chemical reactions, making it a versatile building block for the creation of new molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-Methyl-3-pyridineethanol is used as a reactant for the synthesis of various drugs and drug candidates. Its ability to form a wide range of chemical compounds makes it a valuable starting material for the development of new medications with potential therapeutic benefits.
Used in Chemical Research:
6-Methyl-3-pyridineethanol is also used in chemical research as a model compound to study various chemical reactions and mechanisms. Its unique structure and reactivity make it an interesting subject for researchers looking to understand the behavior of similar compounds and develop new synthetic strategies.
Used in Flavor and Fragrance Industry:
Due to its distinct chemical structure, 6-Methyl-3-pyridineethanol can be used as a building block for the creation of various fragrances and flavors. Its versatility in organic synthesis allows for the development of new and unique scents and tastes that can be used in the production of perfumes, cosmetics, and the food industry.
Used in Material Science:
In the field of material science, 6-Methyl-3-pyridineethanol can be used as a component in the development of new materials with specific properties. Its ability to form a wide range of chemical compounds makes it a valuable resource for researchers looking to create materials with tailored characteristics for various applications, such as in electronics, coatings, or adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 100189-17-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,8 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100189-17:
(8*1)+(7*0)+(6*0)+(5*1)+(4*8)+(3*9)+(2*1)+(1*7)=81
81 % 10 = 1
So 100189-17-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO/c1-7-2-3-8(4-5-10)6-9-7/h2-3,6,10H,4-5H2,1H3
100189-17-1Relevant articles and documents
Hydroboration. 75. Directive Effects in the Hydroboration of Vinyl and Propenyl Heterocycles with Representative Hydroborating Agents
Brown, Herbert C.,Prasad, J. V. N. Vara,Zee, Sheng-Hsu
, p. 439 - 445 (1986)
The hydroboration of representative heterocyclic compounds bearing a vinyl or propenyl substituent with borane-methyl sulfide (BMS), 9-borabicyclononane (9-BBN), dicyclohexylborane (Chx2BH), and disiamylborane (Sia2BH) was investigated systematically to establish directive effects in the hydroboration.The directive effects observed for 2-vinylfuran and 2-vinylthiophene are similar to those realized in styrene.The hydroboration of vinylpyridine required an excess of borane hydroborating agent.Alternatively, the nitrogen atom could be protected by complexing with boron trifluoride.When the vinyl group is ortho or para to the pyridine nitrogen, α-organoboranes are the major products in the hydroboration.However, when the vinyl group is meta to the pyridine nitrogen, β-organoboranes are formed predominantly.Hydroboration of the vinyl-pyridine-BF3 complexes results in an increase in the formation of α-organoboranes, as compared to β.The distribution of boron in the hydroboration of 2-propenyl heterocyclic compounds compared to that of trans-1-propenylbenzene showed that the effect of the heterocycle is pronounced in directing the boron atom strongly to the α-carbon atom.
TETRAAZA-CYCLOPENTA[A]INDENYL DERIVATIVES
-
Page/Page column 141, (2015/01/09)
The present invention provides compounds of Formula (I) as M1 receptor positive allosteric modulators for the treatment of diseases mediated by the muscarinic M1 mediator.
Ruthenium-catalyzed γ-carbolinium ion formation from aryl azides; Synthesis of dimebolin
Dong, Huijun,Latka, Regina T.,Driver, Tom G.
supporting information; experimental part, p. 2726 - 2729 (2011/06/28)
A range of γ-carbolines were produced stereoselectively from ruthenium(III)-catalyzed reactions of 3-pyridyl substituted aryl azides. Other catalysts and conditions were neither as selective nor as high-yielding. This method was used to synthesize dimebolin in a concise and efficient manner.
