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Home Aldehydes 1192-79-6
1192-79-6,MFCD08236773
Catalog No.:AA000I9G

1192-79-6 | 5-Methyl-1h-pyrrole-2-carbaldehyde

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$19.00   $13.00
- +
500mg
95%
in stock  
$32.00   $23.00
- +
1g
95%
in stock  
$52.00   $36.00
- +
  • 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:
AA000I9G
Chemical Name:
5-Methyl-1h-pyrrole-2-carbaldehyde
CAS Number:
1192-79-6
Molecular Formula:
C6H7NO
Molecular Weight:
109.1259
MDL Number:
MFCD08236773
SMILES:
Cc1ccc([nH]1)C=O
NSC Number:
81349
Properties
Properties
 
BP:
226.1°C at 760 mmHg  
Form:
Solid  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
92.5  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
0.9  

Upstream Synthesis Route

[1]OrganicLetters,2006,vol.8,#21,p.4951-4954

[2]Tetrahedron,1993,vol.49,#7,p.1343-1350

[3]Patent:US2016/185786,2016,A1,.Locationinpatent:Paragraph0606

[4]JournalofOrganicChemistry,1980,vol.45,#24,p.4980-4982

[5]JournalofMedicinalChemistry,2004,vol.47,#16,p.4054-4059

[1]Patent:US6982265,2006,B1,.Locationinpatent:Page/Pagecolumn26

[1]OrganicLetters,2006,vol.8,#21,p.4951-4954

[2]Tetrahedron,1993,vol.49,#7,p.1343-1350

[3]TetrahedronLetters,1988,vol.29,#7,p.777-780

[4]TetrahedronLetters,1988,vol.29,#7,p.777-780

[1]Fitoterapia,2002,vol.73,#1,p.22-27

[1]Tetrahedron,1989,vol.45,#11,p.3397-3414

[2]Tetrahedron,1989,vol.45,#11,p.3397-3414

[3]Tetrahedron,1989,vol.45,#11,p.3397-3414

Downstream Synthesis Route

[1]JustusLiebigsAnnalenderChemie,1931,vol.486,p.33

[1]JustusLiebigsAnnalenderChemie,1931,vol.486,p.33

636-41-9    1192-79-6   
dipyrrylmethenehydrochloride 

[1]JournaloftheChemicalSociety.PerkintransactionsII,1980,p.113-116

[1]OrganicLetters,2006,vol.8,p.4951-4954

[2]Tetrahedron,1993,vol.49,p.1343-1350

[3]Patent:US2016/185786,2016,A1.Locationinpatent:Paragraph0606

[4]JournalofOrganicChemistry,1980,vol.45,p.4980-4982

[5]JournalofMedicinalChemistry,2004,vol.47,p.4054-4059

[1]JournaloftheChemicalSociety.PerkintransactionsI,1989,p.909-914

Literature

Title: Chemoenzymatic formation of novel aminocoumarin antibiotics by the enzymes CouN1 and CouN7.

Journal: Biochemistry 20070717

Title: Installation of the pyrrolyl-2-carboxyl pharmacophore by CouN1 and CouN7 in the late biosynthetic steps of the aminocoumarin antibiotics clorobiocin and coumermycin A1.

Journal: Biochemistry 20060718

Title: Metabolic engineering of aminocoumarins: inactivation of the methyltransferase gene cloP and generation of new clorobiocin derivatives in a heterologous host.

Journal: Chembiochem : a European journal of chemical biology 20050801

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SDS
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