Bis(diphenylphosphino)methane - ≥98% , CAS No.2071-20-7

CAS: 2071-20-7 Cat. No.: B101102 Molecular Weight: 384.39 Beilstein Registry Number: 758760 EC Number: 218-194-2

GRADE & PURITY ≥98%

Synonyms

DPPM | AMY11694 | W-107598 | Methylenebis[diphenylphosphine] | 1H-IMIDAZOL-2-OL | (C6H5)2PCH2P(C6H5)2 | [2,2'-Biindan]-1,1'-dione, 2,2',3,3,3',3'-hexahydroxy- | AC-4964 | GC10102 | I5O2HZR38V | 1-Benzyl-3-azetidine-1,3-dicarboxylate | BCP22500 | PHOSPHINE

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyms

DPPM | AMY11694 | W-107598 | Methylenebis[diphenylphosphine] | 1H-IMIDAZOL-2-OL | (C6H5)2PCH2P(C6H5)2 | [2, 2'-Biindan]-1, 1'-dione, 2, 2', 3, 3, 3', 3'-hexahydroxy- | AC-4964 | GC10102 | I5O2HZR38V | 1-Benzyl-3-azetidine-1, 3-dicarboxylate | BCP22500 | PHOSPHINE

Specifications & Purity

≥98%

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488185004
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185004
• Canonical Smiles: C1=CC=C(C=C1)P(CP(C2=CC=CC=C2)C3=CC=CC=C3)C4=CC=CC=C4
• IUPAC Name: diphenylphosphanylmethyl(diphenyl)phosphane
• InChIKey: XGCDBGRZEKYHNV-UHFFFAOYSA-N
• INCHI: 1S/C25H22P2/c1-5-13-22(14-6-1)26(23-15-7-2-8-16-23)21-27(24-17-9-3-10-18-24)25-19-11-4-12-20-25/h1-20H,21H2
• Isomeric SMILES: C1=CC=C(C=C1)P(CP(C2=CC=CC=C2)C3=CC=CC=C3)C4=CC=CC=C4
• WGK Germany: 3
• Molecular Weight: 384.39
• Beilstein: 758760
• Reaxy-Rn: 758760
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=758760&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzene and substituted derivatives
• Alternative Parents: Organic phosphines and derivatives Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic benzene moiety - Phosphine - Organopnictogen compound - Hydrocarbon derivative - Organophosphorus compound - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

Mus musculus (284745 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

B16 (5829 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Insoluble in water
• Sensitivity: Air Sensitive
• Melt Point(°C): 118-122°C
• Molecular Weight: 384.400 g/mol
• XLogP3: 6.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 6
• Exact Mass: 384.12 Da
• Monoisotopic Mass: 384.12 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 27
• Formal Charge: 0
• Complexity: 325.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Bi-Xian Chen, Jing Tan, Yong-Jie Yie, Su-Ru Tang, Xin Deng, Hao-Yuan Xie, Wen-Ting Liu, Xiaojun Liu, Wei-Qin Xu, Chun-Cheng Lin, Sheng-Run Zheng.  (2023)  Pure phase Ni12P5 anchored on N, P-codoped carbon nanosheet: A stable and highly efficient catalyst to reduce toxic organic compounds for continuous-flow application.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2023.157196]

2. Linfeng Zhang, Changpo Ma, Chenyu Wang, Guangyu Sun, Yongqi Shu, Wenya Zou, Tao Yang, Weiran Yang.  (2022)  Direct conversion of glyceric acid to succinic acid by reductive carbonylation.  GREEN CHEMISTRY,  24  (19): (7644-7651).  [PMID:] [10.1039/D2GC02594A]

3. Yuanxin Du, Ji Xiang, Kun Ni, Yapei Yun, Guodong Sun, Xiaoyou Yuan, Hongting Sheng, Yanwu Zhu, Manzhou Zhu.  (2018)  Design of atomically precise Au2Pd6 nanoclusters for boosting electrocatalytic hydrogen evolution on MoS2.  Inorganic Chemistry Frontiers,  5  (11): (2948-2954).  [PMID:] [10.1039/C8QI00697K]

4. Zhuoyuan Li, Chuanjun Zhou, Kaiyang Kuang, Jiahao Liu, Shuang Chen, Shan Jin, Manzhou Zhu.  (2025)  Enhanced Photoluminescence Emission and Thermal Stability in Pt1Ag31 nanocluster from Introduced Secondary Phosphine Oxide Functionalized ligand.  Chemistry-An Asian Journal,      [PMID:40056009] [10.1002/asia.202401819]

5. Lizhong He, Tingting Dong, Xiaoyang Hu, Zibao Gan.  (2024)  Visualizing the fluorescence of AgPt NCs by an asymmetrical pseudo-ligand exchange method.  Inorganic Chemistry Frontiers,      [PMID:] [10.1039/D4QI01275E]