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3-Morpholinone, 2-[(S)-hydroxyphenylmethyl]-4-(phenylmethyl)-, (2R)- is a complex organic compound with the molecular formula C20H21NO3. It is a chiral molecule, meaning it has a non-superimposable mirror image, and the (2R)- notation indicates the specific configuration of the molecule. 3-Morpholinone, 2-[(S)-hydroxyphenylmethyl]-4-(phenylmethyl)-, (2R)- is characterized by a morpholinone ring, which is a five-membered ring containing two nitrogen atoms and one oxygen atom. It features a hydroxyphenylmethyl group attached to the 2-position of the morpholinone ring, and a phenylmethyl group at the 4-position. The compound's structure and properties make it potentially useful in pharmaceutical applications, particularly as a precursor in the synthesis of certain drugs.

800407-90-3

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800407-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 800407-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,0,4,0 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 800407-90:
(8*8)+(7*0)+(6*0)+(5*4)+(4*0)+(3*7)+(2*9)+(1*0)=123
123 % 10 = 3
So 800407-90-3 is a valid CAS Registry Number.

800407-90-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3S)-4-benzyl-2-(hydroxyphenylmethyl)morpholin-3-one

1.2 Other means of identification

Product number -
Other names (2R)-2-[(S)-hydroxy(phenyl)methyl]-4-(phenylmethyl)morpholin-3-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:800407-90-3 SDS

800407-90-3Relevant academic research and scientific papers

Dynamic kinetic resolution-based asymmetric transfer hydrogenation of 2-benzoylmorpholinones and its use in concise stereoselective synthesis of all four stereoisomers of the antidepressant reboxetine

Son, Se-Mi,Lee, Hyeon-Kyu

supporting information, p. 8396 - 8404 (2013/09/24)

Dynamic kinetic resolution-driven, asymmetric transfer hydrogenation reaction of 2-benzoylmorpholin-3-ones (4) proceeds efficiently to give the corresponding (2R,3S)- or (2S,3R)-2-(hydroxyphenylmethyl)morpholin-3-ones (6) with an excellent level of diastereo- and enantioselectivity and simultaneous control of two contiguous stereogenic centers in a single step. This process is employed to prepare all four stereoisomers of the antidepressant reboxetine.

TREATMENT OF PERVASIVE DEVELOPMENTAL DISORDERS WITH NOREPINEPHRINE REUPTAKE INHIBITORS

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Page/Page column 169-170, (2010/02/11)

Provided are methods and medicaments for treating a Pervasive Developmental Disorder, comprising administering to a patient in need of such treatment an effective amount of a selective norepinephrine reuptake inhibitor.

TREATMENT OF HOT FLASHES, IMPULSE CONTROL DISORDERS AND PERSONALITY CHANGE DUE TO A GENERAL MEDICAL CONDITION

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Page/Page column 171-173, (2010/02/12)

Selective norepinephrine reuptake inhibitors are useful for the prevention or treatment of hot flashes, vasomotor symptoms, impulse control disorders or personality change due to a general medical condition.

BENZYL MORPHOLINE DERIVATIVES

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Page 29-30, (2010/02/06)

A compound of formula (I) (I)wherein R is H; Ar is an aromatic group selected from phenyl; X is a phenyl group; R' is H or C1-C4 alkyl; each R1 is independently H or C1-C4 alkyl; and pharmaceutically acceptable salts thereof.

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