64715-81-7 Usage
Uses
Used in Pharmaceutical Production:
(+)-O-METHYL-L-PHENYLALANINOL HYDROCHLORIDE is used as a key intermediate in the synthesis of various pharmaceutical drugs. Its role in creating other chiral molecules makes it an essential component in the development of new medications.
Used in Organic Synthesis:
In the realm of organic synthesis, (+)-O-METHYL-L-PHENYLALANINOL HYDROCHLORIDE is used as a reagent. Its properties allow it to participate in a range of chemical reactions, contributing to the creation of diverse organic chemicals.
Used in Chemical Industry:
(+)-O-METHYL-L-PHENYLALANINOL HYDROCHLORIDE's solubility and reactivity make it a valuable asset in the chemical industry, where it can be incorporated into a variety of chemical processes and products.
Given the provided materials, there are no specific applications detailed for different industries beyond the general uses in pharmaceutical production, organic synthesis, and the chemical industry. If more specific applications are identified in the future, they can be added to the list accordingly.
Check Digit Verification of cas no
The CAS Registry Mumber 64715-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,1 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64715-81:
(7*6)+(6*4)+(5*7)+(4*1)+(3*5)+(2*8)+(1*1)=137
137 % 10 = 7
So 64715-81-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO/c1-12-8-10(11)7-9-5-3-2-4-6-9/h2-6,10H,7-8,11H2,1H3/t10-/m0/s1
64715-81-7Relevant articles and documents
PHENETHYL SUBSTITUTED IMIDAZO[4,5-C]QUINOLINE COMPOUNDS WITH AN N-1 BRANCHED GROUP
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Page/Page column 41, (2020/12/30)
Imidazo[4,5-c]quinoline compounds having a substituent that is attached at the N-1 position by a branched group, single enantiomers of the compounds, pharmaceutical compositions containing the compounds, and methods of making the compounds are disclosed.
The preparation of novel chiral auxiliaries SAMIQ/RAMIQ and their application in the asymmetric Michael addition
Pan, Xuan,Liu, Zhanzhu
, p. 4602 - 4610 (2014/06/23)
A pair of novel chiral auxiliaries SAMIQ/RAMIQ was synthesized from l- or d-phenylalanine methyl ester hydrochloride over six steps in 45.8% and 44.4% yield, respectively. The SAMIQ-/RAMIQ-hydrazone methodology was applied for the asymmetric Michael addit
The dinosyl group: A powerful activator for the regioselective alcoholysis of aziridines
Stanetty, Christian,Blaukopf, Markus K.,Lachmann, Bodo,Noe, Christian R.
supporting information; experimental part, p. 3126 - 3130 (2011/07/08)
The N-2,4-dinitrophenylsulfonyl group (dinosyl, DNs) was found to be an excellent choice for the N-activation of aziridines towards ring cleavage with primary, secondary, andsterically demanding tertiary alcohols. Alcoholysis does not need any additional
