Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II) - ≥98% , CAS No.1375325-71-5

CAS: 1375325-71-5 Cat. No.: C153833 Molecular Weight: 512.41 EC Number: 805-791-3 PubChem CID: 60201440
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
P(t-Bu)3 Pd G2
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
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Size
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250mg
C153833-250mg
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1g
C153833-1g
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5g
C153833-5g
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice 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.

Overview

P(t-Bu)3 Pd G2 (Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)] palladium(II)) is a second generation (G2) precatalyst containing a biphenyl-based ligand. Product participates in various palladium catalyzed cross-coupling reactions, C-C, C-N and C-O bond formation reactions, and Suzuki-Miyaura coupling reactions. It generates active Pd catalyst at room temperature in the presence of weak phosphate or carbonate bases. It has been proposed as an active catalyst for use in Stille reactions of aryl halides (bromides and chlorides).
P(t-Bu)3 Pd G2 (Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)] palladium(II), Pd/P(t-Bu)3) may be used as catalyst in the following studies: . Synthesis of sterically hindered biaryls (tetra-ortho-substituted), via cross-coupling reactions of aryl chlorides. . Stille cross-couplings reactions of aryl chloride. . Synthesis of chloropeptin I, via Stille cross-coupling reaction. . Heck reaction. . Negishi cross-coupling reactions.

Specifications

Synonyms
P(t-Bu)3 Pd G2
Specifications & Purity
≥98%
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Names and Identifiers
Pubchem Sid504771807
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504771807
Canonical SmilesCC(C)(C)P(C(C)(C)C)C(C)(C)C.C1=CC=C([C-]=C1)C2=CC=CC=C2N.Cl[Pd+]
IUPAC Namechloropalladium(1+);2-phenylaniline;tritert-butylphosphane
InChIKeyDZNFQIYYEXFFGV-UHFFFAOYSA-M
INCHI1S/C12H10N.C12H27P.ClH.Pd/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-10(2,3)13(11(4,5)6)12(7,8)9;;/h1-6,8-9H,13H2;1-9H3;1H;/q-1;;;+2/p-1
Isomeric SMILES CC(C)(C)P(C(C)(C)C)C(C)(C)C.C1=CC=C([C-]=C1)C2=CC=CC=C2N.Cl[Pd+]
WGK Germany 3
PubChem CID 60201440
Molecular Weight 512.41
Reaxy-Rn 22750896

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.

View spec sheet →

Advanced Data

3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeDateItem
F2418351Certificate of AnalysisJun 12, 2024 C153833
F2418352Certificate of AnalysisJun 12, 2024 C153833
F2418353Certificate of AnalysisJun 12, 2024 C153833
F2418354Certificate of AnalysisJun 12, 2024 C153833
F2418355Certificate of AnalysisJun 12, 2024 C153833
F2418356Certificate of AnalysisJun 12, 2024 C153833
J2530112Certificate of AnalysisJun 12, 2024 C153833
Chemical and Physical Properties
SensitivityAir and moisture sensitive
Melt Point(°C)167-170°C
Solution Calculators
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