3-phenyl-CPP - Moligand™ , Channel blocker of ClC-Ka;Channel blocker of ClC-Kb, CAS No.P607172, Channel blocker of ClC-Ka;Channel blocker of ClC-Kb

CAS: P607172 Cat. No.: P607172 PubChem CID: 10356116
AVAILABLE TO ORDER
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.
Synonyms
GTPL4104 | EN300-43356163 | 2-(4-chlorophenoxy)-3-phenylpropanoic acid | SCHEMBL20553475 | Q27073745 | 3-phenyl-CPP | 2-(p-chlorophenoxy)-3-phenylpropionic acid | PD051097
Storage
Room temperature
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5mg
P607172-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$1,000.90
25mg
P607172-25mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$1,714.90

$2,000.90
Save $286.00 (14.29%)
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Why this grade

Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
GTPL4104 | EN300-43356163 | 2-(4-chlorophenoxy)-3-phenylpropanoic acid | SCHEMBL20553475 | Q27073745 | 3-phenyl-CPP | 2-(p-chlorophenoxy)-3-phenylpropionic acid | PD051097
Specifications & Purity
Moligand™
Storage
Room temperature
Grade
Moligand™
Action Type
CHANNEL BLOCKER
Mechanism of action
Channel blocker of ClC-Ka;Channel blocker of ClC-Kb
Names and Identifiers
Canonical SmilesOC(=O)C(Cc1ccccc1)Oc1ccc(cc1)Cl
IUPAC Name2-(4-chlorophenoxy)-3-phenylpropanoic acid
InChIKeyCPBLTMSKPQDJPW-UHFFFAOYSA-N
INCHI1S/C15H13ClO3/c16-12-6-8-13(9-7-12)19-14(15(17)18)10-11-4-2-1-3-5-11/h1-9,14H,10H2,(H,17,18)
Isomeric SMILES C1=CC=C(C=C1)CC(C(=O)O)OC2=CC=C(C=C2)Cl
PubChem CID 10356116

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassPhenoxyacetic acid derivatives
Intermediate Tree Nodes Not available
Direct ParentPhenoxyacetic acid derivatives
Alternative Parents Phenylpropanoic acids  Phenoxy compounds  Phenol ethers  Chlorobenzenes  Alkyl aryl ethers  Aryl chlorides  Monocarboxylic acids and derivatives  Carboxylic acids  Organochlorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents 3-phenylpropanoic-acid - Phenoxyacetate - Phenoxy compound - Phenol ether - Alkyl aryl ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Organooxygen compound - Organic oxygen compound - Carbonyl group - Organic oxide - Organochloride - Hydrocarbon derivative - Organohalogen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as phenoxyacetic acid derivatives. These are compounds containing an anisole where the methane group is linked to an acetic acid or a derivative.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CLCNKB Tchem Chloride channel protein ClC-Kb (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CLCNKA Tchem Chloride channel protein ClC-Ka (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Solution Calculators
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