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(3,4-dihydro-2H-pyrano[2,3-b]pyridin-6-yl)methanol is a chemical compound characterized by a pyrano-pyridine ring system and a methanol group. It is a promising candidate for pharmaceutical and medicinal applications, particularly in drug discovery research.
Used in Pharmaceutical Industry:
(3,4-dihydro-2H-pyrano[2,3-b]pyridin-6-yl)methanol is used as a potential drug candidate for its unique structure and properties, which make it an interesting target for therapeutic development.
Used in Medicinal Chemistry:
(3,4-dihydro-2H-pyrano[2,3-b]pyridin-6-yl)methanol is used as a building block in the synthesis of other organic compounds, contributing to the advancement of medicinal chemistry and drug development.
Used in Drug Discovery Research:
(3,4-dihydro-2H-pyrano[2,3-b]pyridin-6-yl)methanol is used as a target for drug discovery research due to its potential in a range of therapeutic areas and its biological activities.

1346446-87-4

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1346446-87-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1346446-87-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,4,4 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1346446-87:
(9*1)+(8*3)+(7*4)+(6*6)+(5*4)+(4*4)+(3*6)+(2*8)+(1*7)=174
174 % 10 = 4
So 1346446-87-4 is a valid CAS Registry Number.

1346446-87-4Downstream Products

1346446-87-4Relevant academic research and scientific papers

Synthesis method of (3,4-dihydro-2H-pyrano[2,3-b]pyridin-6-yl)methanol

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, (2020/02/14)

The invention discloses a synthesis method of a (3,4-dihydro-2H-pyrano[2,3-b]pyridin-6-yl)methanol compound. Methyl 6-hydroxy-5-iodonicotinate which is used as an initial raw material undergoes a chlorination reaction, and the obtained reaction product and tert-butyl dimethyl(prop-2-alkynyloxy)silane undergo an alkyne substitution reaction, an alkynyl reduction reaction, a TBS protection removal reaction, a cyclization reaction and reduction to obtain the target compound. The synthesis method of the (3,4-dihydro-2H-pyrano[2,3-b]pyridin-6-yl)methanol fills the blank of synthesis methods in theprior art, and the method adopting the above whole synthesis route has the advantages of good step repeatability, high conversion rate, high yield, easiness in purification, mild reaction conditions,high safety, greenness and environmental friendliness; and the obtained 4-fluoro-3-substituted-pyridine-2-formate product compound has the advantages of high purity, good quality, and facilitation ofrealization of industrialization.

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