4-Chloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine

Name: 4-Chloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine
Brand: ChemScene
Availability: InStock
Rating: 5 (1 reviews)

CAS No. 7781-10-4
Cat. No. CS-W019215
Purity≥98%
MDL No.None

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4-Chloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine|CS-W019215

Structure of 7781-10-4

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Description

4-Chloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine is a heterocyclic building block featuring a chlorine substituent at the C4 position and a methyl group at C7. This electron-deficient scaffold integrates readily into kinase inhibitor scaffolds and other bioactive molecules due to its planar structure and compatibility with palladium-catalyzed cross-coupling reactions. The compound exhibits bench-stable handling characteristics under standard conditions.

Application

4-Chloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine serves as a versatile building block for purine-derived scaffolds in medicinal chemistry. Its chloro group enables palladium-catalyzed cross-coupling reactions, while the methyl substituent enhances metabolic stability. The heterocyclic core exhibits excellent bench stability and compatibility with diverse functional groups, facilitating efficient synthesis of kinase inhibitors and nucleoside analogs.

General Information

CAS No. 7781-10-4
Cat. No. CS-W019215
Purity ≥98%
MDL No. None
Storage -20°C, stored under nitrogen
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₇H₆ClN₃
Molecular Weight 167.60
Synonym(s) NSC 102340
SMILES C2=CC1=C(N=CN=C1[N]2C)Cl

Computational Chemistry Data

TPSA 30.71
LogP 1.6217
H_Acceptors 3
H_Donors 0
Rotatable_Bonds 0

Safety Information

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GHS Pictogram :	GHS No : GHS06
Signal Word : Danger	UN#: 2811
Class : 6.1	Packing Group : Ⅲ
Hazard Statements : H301
Precautionary Statements : P264-P270-P330-P405-P501

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Other Classifications

Building Blocks Skeleton Aromatic heterocycle compounds Pyrrole compounds

Building Blocks Skeleton Aromatic heterocycle compounds Pyrimidine compounds

Key Words

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4-Chloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine

CAS No. 7781-10-4

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