Home Deuterated Building Blocks 4441-30-9
4441-30-9,MFCD01713533
Catalog No.:AA0037RZ

4441-30-9 | 3-Morpholinopropanol

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1g
98%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$9.00   $7.00
- +
10g
98%
in stock  
$12.00   $8.00
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25g
98%
in stock  
$15.00   $11.00
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100g
98%
in stock  
$57.00   $40.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0037RZ
Chemical Name:
3-Morpholinopropanol
CAS Number:
4441-30-9
Molecular Formula:
C7H15NO2
Molecular Weight:
145.1995
MDL Number:
MFCD01713533
SMILES:
OCCCN1CCOCC1
Properties
Computed Properties
 
Complexity:
81.7  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
-0.4  

Upstream Synthesis Route

[1]Patent:CN106045942,2016,A,.Locationinpatent:Paragraph0023;0020

[2]Patent:CN103382206,2016,B,.Locationinpatent:Paragraph0235-0238

[3]JournalofMedicinalChemistry,2004,vol.47,#4,p.871-887

[4]Patent:WO2004/108677,2004,A1,.Locationinpatent:Page141

[5]Patent:US6265411,2001,B1,

[6]Patent:US6291455,2001,B1,

[7]Patent:US6294532,2001,B1,

[8]Patent:EP1171440,2004,B1,.Locationinpatent:Page50

[1]Patent:US6291455,2001,B1,

[1]JournalofOrganicChemistry,1955,vol.20,p.855,858

[2]JournaloftheAmericanChemicalSociety,1942,vol.64,p.970,972

[3]Pharmazie,1959,vol.14,p.201,202

[4]JournaloftheAmericanChemicalSociety,1949,vol.71,p.3366,3368

[5]JournaloftheAmericanChemicalSociety,1949,vol.71,p.3366,3368

[6]JournaloftheAmericanPharmaceuticalAssociation(1912-1977),1951,vol.40,p.373,375

[7]BioorganicandMedicinalChemistry,2015,vol.23,#21,p.6875-6884

[8]Patent:US2795581,1955,,

[1]JournalofPharmaceuticalSciences,1994,vol.83,#5,p.644-648

[2]BioorganicandMedicinalChemistryLetters,2013,vol.23,#4,p.1036-1040

[1]Tetrahedron,2007,vol.63,#52,p.12903-12911

Downstream Synthesis Route

[1]JournaloftheAmericanPharmaceuticalAssociation(1912),39<1950,4,5,

[1]Tetrahedron,2007,vol.63,p.12903-12911

[2]JournaloftheAmericanChemicalSociety,1957,vol.79,p.5667,5670

[3]PharmaceuticalChemistryJournal,1967,p.463-467    Khimiko-FarmatsevticheskiiZhurnal,1967,p.35-39

[4]Patent:US2009/124624,2009,A1.Locationinpatent:Page/Pagecolumn22

[5]BioorganicandMedicinalChemistry,2015,vol.23,p.6875-6884

[6]Patent:US2795581,1955,

[1]Baboulene,Michel;Torregrosa,Jean-Luc;Speziale,Vincent;Lattes,Armand[BulletindelaSocieteChimiquedeFrance,1980,vol.2,#11-12,p.565-570]

[1]Heravi,MajidM.;Ajami,Dariush;Tabar-Heydar,Kourosh[MonatsheftefurChemie,1998,vol.129,#12,p.1305-1308]

[1]JournalofMedicinalChemistry,2000,vol.43,p.1380-1397

[2]Patent:US6344459,2002,B1.Locationinpatent:Pagecolumn53-54

Literature

Title: Expression of verotoxin-1 receptor Gb3 in breast cancer tissue and verotoxin-1 signal transduction to apoptosis.

Journal: BMC cancer 20090101

Title: A specific and sensitive assay for gefitinib using the enzyme-linked immunosorbent assay in human serum.

Journal: Biological & pharmaceutical bulletin 20051001

Title: Optimization of 4-phenylamino-3-quinolinecarbonitriles as potent inhibitors of Src kinase activity.

Journal: Journal of medicinal chemistry 20011108

Title: Synthesis and Src kinase inhibitory activity of a series of 4-phenylamino-3-quinolinecarbonitriles.

Journal: Journal of medicinal chemistry 20010301

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Tags:4441-30-9 Molecular Formula|4441-30-9 MDL|4441-30-9 SMILES|4441-30-9 3-Morpholinopropanol