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(R)-2-Methyl-morpholine is a chiral organic compound belonging to the morpholine family. It is characterized by its asymmetric carbon atom, which gives it a specific stereochemistry. (R)-2-Methyl-morpholine is known for its unique properties and reactivity, making it a valuable building block in the synthesis of various pharmaceuticals and organic compounds.

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  • 168038-14-0 Structure
  • Basic information

    1. Product Name: (R)-2-Methyl-morpholine
    2. Synonyms: (R)-2-Methylmorpholine HCl;(R)-2-Methylmorpholine hydrochloride;(2R)-2-MethylMorpholine;Morpholine,2-Methyl-, hydrochloride (1:1), (2R)-;(R)-2-MethylMorpholine (N-Boc protected);(2R)-2-Methylmorpholine hydrochloride
    3. CAS NO:168038-14-0
    4. Molecular Formula: C5H11NO
    5. Molecular Weight: 101.14694
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 168038-14-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 137.1ºC at 760 mmHg
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.891 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-2-Methyl-morpholine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-Methyl-morpholine(168038-14-0)
    11. EPA Substance Registry System: (R)-2-Methyl-morpholine(168038-14-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 168038-14-0(Hazardous Substances Data)

168038-14-0 Usage

Uses

Used in Pharmaceutical Industry:
(R)-2-Methyl-morpholine is used as a reactant in the preparation of naphthyridine as a hedgehog protein modulator. It plays a crucial role in the synthesis process, where it is derived from chloronicotinonitrile via aryl amination of naphthyridine halide. This application is significant in the development of drugs targeting the hedgehog signaling pathway, which is implicated in various diseases, including cancer and congenital disorders.
Additionally, due to its unique properties and reactivity, (R)-2-Methyl-morpholine can be employed as a building block or intermediate in the synthesis of other pharmaceuticals and organic compounds. Its chiral nature and ability to form stable complexes with various functional groups make it a versatile component in the design and development of new drugs and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 168038-14-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,0,3 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 168038-14:
(8*1)+(7*6)+(6*8)+(5*0)+(4*3)+(3*8)+(2*1)+(1*4)=140
140 % 10 = 0
So 168038-14-0 is a valid CAS Registry Number.

168038-14-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-Methylmorpholine hydrochloride

1.2 Other means of identification

Product number -
Other names (R)-2-Methyl-morpholine

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:168038-14-0 SDS

168038-14-0Relevant articles and documents

PYRAZOLO[3,4-D]PYRIMIDIN DERIVATIVE AND ITS USE FOR THE TREATMENT OF LEISHMANIASIS

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Page/Page column 37, (2016/08/17)

The compound 3,3,3-trifluoro-N-((1,4-trans)-4-((3-((S)-2-methylmorpholino)-1H- pyrazolo[3,4-d]pyrimidin-6-yl)amino)cyclohexyl)propane-1-sulfonamidehaving the Formula (I) or a salt thereof, its opposite enantiomer, compositions comprising the compound and its use in the treatment or prevention of leishmaniasis, particularly visceral leishmaniasis.

CHROMENONE COMPOUNDS AS PI 3 -KINASE INHIBITORS FOR THE TREATMENT OF CANCER

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, (2012/11/06)

The invention concerns chromenone compounds of Formula I; or pharmaceutically-acceptable salts thereof, wherein each of R1, R2, R3, R4, R5, n and R6 has any of the meanings defined hereinbe

CHROMENONE DERIVATIVES

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, (2012/10/23)

The invention concerns chromenone compounds of Formula I; or pharmaceutically-acceptable salts thereof, wherein each of R1, R2, R3, R4, R5, n and R6 has any of the meanings defined hereinbe

THIAZOLOPYRIMIDINONE DERIVATIVES AS PI3 KINASE INHIBITORS

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Page/Page column 47, (2010/12/18)

This invention relates to the use of thiazolopyrimidinone derivatives for the modulation, notably the inhibition of the activity or function of the phosphoinositide 3' OH kinase family (hereinafter PI3 kinases), suitably, PI3Kα, PI3Kδ, PI3Kβ, and/or PI3Kγ

COMPOUNDS AND COMPOSITIONS AS KINASE INHIBITORS

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Page/Page column 116-117, (2009/09/05)

The invention provides a novel class of 2,7-naphthyridin derivatives; pharmaceutical compositions comprising such compounds and methods of using such compounds to treat o prevent diseases or disorders associated with abnormal or deregulated kinase activit

COMPOUNDS AND COMPOSITIONS AS HEDGEHOG PATHWAY MODULATORS

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Page/Page column 33-34, (2008/06/13)

The invention provides a method for modulating the activity of the hedgehog signaling pathway. In particular, the invention provides a method for inhibiting aberrant growth states resulting from phenotypes such as Ptc loss-of-function, hedgehog gain-of-fu

Compounds and compositions as inhibitors of receptor tyrosine kinase activity

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Page/Page column 16-18, (2010/02/11)

The invention provides a novel class of compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with cSRC, Lck, FGFR3, Flt3, TrkB, Bmx, and/or PFGFRα kinase

Quinolinecarboxylic acid derivatives, antibacterial agent containing the same

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, (2008/06/13)

Novel quinolinecarboxylic acid derivatives of the formula: STR1 wherein Z is STR2 or STR3 in which R1 is hydrogen atom, a halogen atom, hydroxy or a lower alkyloxy; R2 is a halogen atom, hydroxy or a lower alkyloxy; R3 is a lower alkyl; and R4 is hydroxy or a di(lower alkyl)amino, and a pharmaceutically acceptable salt thereof, which have excellent antibacterial activities and are useful as an antibacterial agent, a pharmaceutical composition containing the same, and process for preparing the same.

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