34723-82-5 Usage
Description
2-(Bromomethyl)tetrahydro-2H-pyran is a colorless to yellow liquid that has been investigated for its cross-coupling reaction with potassium heteroaryltrifluoroborates. 2-(BROMOMETHYL)TETRAHYDRO-2 H-PYRAN is known for its role in the preparation of tellurated heterocycles, which are important in various chemical and pharmaceutical applications.
Uses
Used in Chemical Synthesis:
2-(Bromomethyl)tetrahydro-2H-pyran is used as a key intermediate in the synthesis of tellurated heterocycles, such as 2-[(2-thienyltelluro)methyl]tetrahydrofuran and [(2-thienyltelluro)methyl]tetrahydro-2H-pyran. These heterocycles are valuable for their unique chemical properties and potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(Bromomethyl)tetrahydro-2H-pyran is used as a building block for the development of new drugs. Its ability to form tellurated heterocycles makes it a promising candidate for the creation of novel therapeutic agents with potential applications in treating various diseases.
Used in Material Science:
2-(Bromomethyl)tetrahydro-2H-pyran is also utilized in the field of material science for the development of new materials with unique properties. The tellurated heterocycles derived from this compound can be used to create advanced materials with improved performance in areas such as electronics, optics, and energy storage.
Check Digit Verification of cas no
The CAS Registry Mumber 34723-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,2 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34723-82:
(7*3)+(6*4)+(5*7)+(4*2)+(3*3)+(2*8)+(1*2)=115
115 % 10 = 5
So 34723-82-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H11BrO/c7-5-6-3-1-2-4-8-6/h6H,1-5H2
34723-82-5Relevant articles and documents
A new simple and industrial process for bromination of alcohols
Mas,Metivier
, p. 2187 - 2191 (2007/10/02)
Alcohols treated with thionylchloride, followed by chlorine/bromine exchange using gaseous hydrobromic acid and thermal decomposition in the presence of a tertiary amine give the corresponding brominated compounds. The process is regio/stereo selective.