1H-Pyrrolo[3,2-c]pyridine-3-carboxaldehyde

Name: 1H-Pyrrolo[3,2-c]pyridine-3-carboxaldehyde
Brand: ChemScene
Availability: InStock
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CAS No. 933717-10-3
Cat. No. CS-D1656
Purity≥95%
MDL No.MFCD08690128

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Type	HazMat Fee
Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
Hazmat Ground shipping	$50.00+
Inaccessible (Haz class 6.1 or 9), Domestic	$68.00+
Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
Inaccessible (Haz class 6.1 or 9), International	$108.00+
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1H-Pyrrolo[3,2-c]pyridine-3-carboxaldehyde|CS-D1656

Structure of 933717-10-3

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General Information

CAS No. 933717-10-3
Cat. No. CS-D1656
Purity ≥95%
MDL No. MFCD08690128
Storage 4°C, stored under nitrogen
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₈H₆N₂O
Molecular Weight 146.15
Synonym(s) 1H-Pyrrolo[2,3-c]pyridine-3-carboxaldehyde
SMILES O=CC1=CNC2=C1C=NC=C2

Description

1H-Pyrrolo[3,2-c]pyridine-3-carboxaldehyde features a fused heterocyclic core with a strategically positioned aldehyde group, enabling direct functionalization in transition metal-catalyzed couplings and multicomponent reactions. The electron-deficient pyrrole ring enhances reactivity in electrophilic transformations, while the aldehyde serves as a key handle for conjugation. This scaffold supports rapid access to bioactive molecules in medicinal chemistry and materials science applications.

Application

1H-Pyrrolo[3,2-c]pyridine-3-carboxaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds via standard aldehyde transformations. Its conjugated system imparts stability and facilitates electrophilic reactions, while the aldehyde group supports reductive amination, cyanation, and coupling protocols. The molecule exhibits excellent bench stability and is compatible with common protecting group strategies, making it ideal for iterative synthesis campaigns in API development.

Synthesis

Route1
- In-stock
  
  271-34-1
- 4885-02-3
- ~%
- In-stock
  
  933717-10-3
References
- KATHOLIEKE UNIVERSITEIT LEUVEN; BARDIOT, Dorothée; CARLENS, Gunter; DALLMEIER, Kai; KAPTEIN, Suzanne; McNAUGHTON, Michael; MARCHAND, Arnaud; NEYTS, Johan; SMETS, Wim Patent: WO2013/45516 A1, 2013 ; Location in patent: Page/Page column 201 ;

Safety Information

Download SDS

GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

TPSA 45.75
LogP 1.3754
H_Acceptors 2
H_Donors 1
Rotatable_Bonds 1

Other Classifications

Building Blocks Skeleton Aromatic heterocycle compounds Pyridine compounds

Building Blocks Skeleton Aromatic heterocycle compounds Pyrrole compounds

Key Words

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1H-Pyrrolo[3,2-c]pyridine-3-carboxaldehyde

CAS No. 933717-10-3

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