34154-81-9 Usage
Description
Benzenemethanol, a-[1-(diethylamino)ethyl]-,(R,R)(9CI) is an organic compound with a complex structure, featuring a benzene ring, a methanol group, and a diethylaminoethyl group. It is characterized by its chiral centers (R,R), which give it unique stereochemical properties. Benzenemethanol, a-[1-(diethylamino)ethyl]-,(R,R)(9CI) is primarily known as a metabolite of Diethylpropione, a substance with various applications in different industries.
Uses
Used in Pharmaceutical Industry:
Benzenemethanol, a-[1-(diethylamino)ethyl]-,(R,R)(9CI) is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and chiral properties make it a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, Benzenemethanol, a-[1-(diethylamino)ethyl]-,(R,R)(9CI) serves as a key compound for studying the properties and reactivity of chiral molecules. Its synthesis and manipulation can provide insights into the development of novel synthetic methods and the understanding of stereoselective reactions.
Used in Analytical Chemistry:
As a chiral compound, Benzenemethanol, a-[1-(diethylamino)ethyl]-,(R,R)(9CI) can be employed as a reference material in analytical chemistry. It can be used to calibrate and validate chromatographic and spectroscopic methods, ensuring the accurate determination of enantiomeric purity and the study of stereoselective processes.
Check Digit Verification of cas no
The CAS Registry Mumber 34154-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,5 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34154-81:
(7*3)+(6*4)+(5*1)+(4*5)+(3*4)+(2*8)+(1*1)=99
99 % 10 = 9
So 34154-81-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H21NO/c1-4-14(5-2)11(3)13(15)12-9-7-6-8-10-12/h6-11,13,15H,4-5H2,1-3H3/t11-,13+/m0/s1
34154-81-9Relevant articles and documents
THE STEREOSELECTIVE REDUCTION OF α-AMINOPROPIOPHENONE DERIVATIVES WITH SODIUM BOROHYDRIDE
Kametani, Tetsuji,Kigasawa, Kazuo,Hiiragi, Mineharu,Wagatsuma, Nagatoshi,Kohagizawa, Toshitaka,Inoue, Hitoshi
, p. 775 - 778 (2007/10/02)
The ratio of erythro and threo products from the sodium borohydride reduction of the hydrochlorides, and other acid salts, of α-aminopropiophenone derivatives was determined.It was found that this procedure resulted in stereoselective formation of erythro-2-amino-1-phenylpropanols in contrast to sodium borohydride reduction of the corresponding free bases.The method was successfully applied to the synthesis of dl-erythro-2-(4-benzylpiperidino)-1-(4-hydroxyphenyl)propanol which has been used as a vasodilator.