1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 4-chloro- 4-chloro-1h-pyrrolo[2,3-b]pyridine-5-carbaldehyde 4-chloro-1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 4-chloro-5-formyl-1h-pyrrolo[2,3-b]pyridine 4-chloro-7-azaindole-5-carboxaldehyde 4-chloro1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde 958230-19-8 anti-N-Cbz-7-hydroxy-2-azabicyclo[2.2.1]heptane CAS 958230-19-8

Purity 97%+In StockPharmaceutical Standards
CAS No.958230-19-8
Molecular FormulaC8H13ClN2O
Molecular Weight188.65 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 4-chloro-
4-chloro-1h-pyrrolo[2,3-b]pyridine-5-carbaldehyde
4-chloro-1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 4-chloro-5-formyl-1h-pyrrolo[2,3-b]pyridine
4-chloro-7-azaindole-5-carboxaldehyde
4-chloro1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde
958230-19-8
anti-N-Cbz-7-hydroxy-2-azabicyclo[2.2.1]heptane CAS 958230-19-8 chemical structure

Description

The occurrence of 1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 4-chloro- 4-chloro-1h-pyrrolo[2,3-b]pyridine-5-carbaldehyde 4-chloro-1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 4-chloro-5-formyl-1h-pyrrolo[2,3-b]pyridine 4-chloro-7-azaindole-5-carboxaldehyde 4-chloro1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde 958230-19-8 anti-N-Cbz-7-hydroxy-2-azabicyclo[2.2.1]heptane is closely related to an amide group, a hydroxyl group, an ether linkage, chlorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 4-chloro- 4-chloro-1h-pyrrolo[2,3-b]pyridine-5-carbaldehyde 4-chloro-1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 4-chloro-5-formyl-1h-pyrrolo[2,3-b]pyridine 4-chloro-7-azaindole-5-carboxaldehyde 4-chloro1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde 958230-19-8 anti-N-Cbz-7-hydroxy-2-azabicyclo[2.2.1]heptane (CAS 958230-19-8), molecular formula C8H13ClN2O and molecular weight 188.65 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 4-chloro- 4-chloro-1h-pyrrolo[2,3-b]pyridine-5-carbaldehyde 4-chloro-1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 4-chloro-5-formyl-1h-pyrrolo[2,3-b]pyridine 4-chloro-7-azaindole-5-carboxaldehyde 4-chloro1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde 958230-19-8 anti-N-Cbz-7-hydroxy-2-azabicyclo[2.2.1]heptane (C8H13ClN2O) contains an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 3.0, corresponding to approximately 3 ring(s) or double-bond equivalent(s). With a molecular weight of 188.65 g/mol, it falls into the medium-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 4-chloro- 4-chloro-1h-pyrrolo[2,3-b]pyridine-5-carbaldehyde 4-chloro-1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 4-chloro-5-formyl-1h-pyrrolo[2,3-b]pyridine 4-chloro-7-azaindole-5-carboxaldehyde 4-chloro1h-pyrrolo[2,3-b]pyridine-5-carboxaldehyde 958230-19-8 anti-N-Cbz-7-hydroxy-2-azabicyclo[2.2.1]heptane under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC8H13ClN2O
Molecular Weight188.65 g/mol
AppearanceWhite to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms2

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