1071436-31-1 Usage
General Description
(R)-3-(4-Methoxyphenyl)-beta-alaninol, also known as (R)-3-(4-Methoxyphenyl)alaninol, is a chemical compound with the molecular formula C10H15NO3. It is also known by its trade name L-759274 and is a selective beta-3 adrenergic receptor agonist. (R)-3-(4-METHOXYPHENYL)-BETA-ALANINOL is being studied for its potential use in the treatment of obesity and metabolic disorders. It works by targeting and activating the beta-3 adrenergic receptors, which are involved in the regulation of lipolysis and thermogenesis. This action can potentially lead to increased energy expenditure and fat burning, making it a promising candidate for the development of new weight management therapies. Additionally, (R)-3-(4-Methoxyphenyl)-beta-alaninol may also have other potential pharmaceutical applications, making it a subject of ongoing research in the fields of pharmacology and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1071436-31-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,1,4,3 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1071436-31:
(9*1)+(8*0)+(7*7)+(6*1)+(5*4)+(4*3)+(3*6)+(2*3)+(1*1)=121
121 % 10 = 1
So 1071436-31-1 is a valid CAS Registry Number.
InChI:InChI=1S/C10H15NO2/c1-13-9-4-2-8(3-5-9)10(11)6-7-12/h2-5,10,12H,6-7,11H2,1H3/t10-/m1/s1
1071436-31-1Relevant articles and documents
Base-induced Sommelet–Hauser rearrangement of N-(α-(2-oxyethyl)branched)benzylic glycine ester-derived ammonium salts via a chelated intermediate
Baba, Souya,Hirano, Kazuki,Tayama, Eiji
supporting information, (2020/03/13)
The base-induced Sommelet–Hauser (S–H) rearrangement of N-(α-branched)benzylic glycine ester-derived ammonium salts 1 was investigated. When the α-branched substituent was a simple alkyl, such as a methyl or butyl, desired S–H rearrangement product 2 was obtained in low yield with formation of the [1,2] Stevens rearranged 4 and Hofmann eliminated products 5 and 6. However, when the α-branched substituent had a 2-oxy moiety, such as 2-acetoxyethyl or 2-benzoyloxyethyl, the yields of 2 were improved. These results could be explained by formation of chelated intermediate C that stabilizes the carbanionic ylide, and the subsequent initial dearomative [2,3] sigmatropic rearrangement would be accelerated. The existence of C was supported by mechanistic experiments. This enhancement effect is not very strong or effective; however, it will expand the synthetic usefulness of ammonium ylide rearrangements.
(S) 3 p Methoxyphenyl 3 acetylaminopropan 1 ol, a new metabolite of an actinomycete
Keller-Schierlein,Klaus,Naegeli,Wolf,Zaehner
, p. 1001 - 1002 (2007/10/05)
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