70187-32-5,MFCD00005947
Catalog No.:AA0036PD

70187-32-5 | 4-Methylmorpholine N-oxide monohydrate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$12.00   $8.00
- +
25g
98%
in stock  
$19.00   $13.00
- +
100g
98%
in stock  
$39.00   $27.00
- +
500g
98%
in stock  
$172.00   $120.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Application
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0036PD
Chemical Name:
4-Methylmorpholine N-oxide monohydrate
CAS Number:
70187-32-5
Molecular Formula:
C5H13NO3
Molecular Weight:
135.1616
MDL Number:
MFCD00005947
SMILES:
[O-][N+]1(C)CCOCC1.O
Properties
Properties
 
Form:
Solid  
MP:
71-75 °C  
Stability:
Hygroscopic  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
78.5  
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  

Downstream Synthesis Route

[1]CurrentPatentAssignee:AMGENINC-US2003/144286,2003,A1

[1]CurrentPatentAssignee:PARIONSCIENCESINC-US2003/199456,2003,A1

[1]CurrentPatentAssignee:BASFSE-US5254717,1993,A

methyl2-(m-bromomethylphenyl)-3-methoxyacrylate 
  70187-32-5   
methyl2-(m-formylphenyl)-3-methoxyacrylate 

[1]CurrentPatentAssignee:BASFSE-US5286750,1994,A

156934-60-0    70187-32-5   
2-(1,2-Dihydroxyethyl)-5-methyl-2,3,6,7-tetrahydrofuro-2,3-fquinoline-7-one 

[1]CurrentPatentAssignee:KOWACOMPANY,LTD.-US5576324,1996,A

Literature
Application
4-Methylmorpholine N-oxide (MNO) monohydrate serves as a versatile reagent in chemical reactions. It participates in the dihydroxylation and aminohydroxylation of olefins when employed with osmium tetroxide (OsO4) catalyst. Additionally, it facilitates the selective oxidation of sulphides to sulfoxides or sulfones in the presence of manganese and copper complexes with tetradentate ligands.
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Additional Info:
SDS
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Tags:70187-32-5 Molecular Formula|70187-32-5 MDL|70187-32-5 SMILES|70187-32-5 4-Methylmorpholine N-oxide monohydrate
Catalog No.: AA0036PD
70187-32-5,MFCD00005947
70187-32-5 | 4-Methylmorpholine N-oxide monohydrate
Pack Size: 5g
Purity: 98%
in stock
$12.00 $8.00
Pack Size: 25g
Purity: 98%
in stock
$19.00 $13.00
Pack Size: 100g
Purity: 98%
in stock
$39.00 $27.00
Pack Size: 500g
Purity: 98%
in stock
$172.00 $120.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0036PD
Chemical Name: 4-Methylmorpholine N-oxide monohydrate
CAS Number: 70187-32-5
Molecular Formula: C5H13NO3
Molecular Weight: 135.1616
MDL Number: MFCD00005947
SMILES: [O-][N+]1(C)CCOCC1.O
Properties
Form: Solid  
MP: 71-75 °C  
Stability: Hygroscopic  
Storage: Keep in dry area;2-8℃;  
Complexity: 78.5  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
Downstream Synthesis Route
114615-82-6    509094-02-4    70187-32-5    509094-03-5 

[1]CurrentPatentAssignee:AMGENINC-US2003/144286,2003,A1

587880-26-0    70187-32-5    587880-27-1 

[1]CurrentPatentAssignee:PARIONSCIENCESINC-US2003/199456,2003,A1

115199-26-3    70187-32-5    133840-49-0 

[1]CurrentPatentAssignee:BASFSE-US5254717,1993,A

methyl2-(m-bromomethylphenyl)-3-methoxyacrylate 
  70187-32-5   
methyl2-(m-formylphenyl)-3-methoxyacrylate 

[1]CurrentPatentAssignee:BASFSE-US5286750,1994,A

156934-60-0    70187-32-5   
2-(1,2-Dihydroxyethyl)-5-methyl-2,3,6,7-tetrahydrofuro-2,3-fquinoline-7-one 

[1]CurrentPatentAssignee:KOWACOMPANY,LTD.-US5576324,1996,A

Application fold
4-Methylmorpholine N-oxide (MNO) monohydrate serves as a versatile reagent in chemical reactions. It participates in the dihydroxylation and aminohydroxylation of olefins when employed with osmium tetroxide (OsO4) catalyst. Additionally, it facilitates the selective oxidation of sulphides to sulfoxides or sulfones in the presence of manganese and copper complexes with tetradentate ligands.
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