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Tricyclohexylphosphine solution - 20 wt. % in toluene, high purity , CAS No.2622-14-2

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Tricyclohexylphosphine solution - 20 wt. % in toluene, high purity , CAS No.2622-14-2

6 Citations

COA

Grade & Purity:

20 wt. % in toluene

Cas Number: 2622-14-2
Molecular Weight: 280.43
Beilstein Registry Number: 957171
EC Number: 220-069-2
PubChem CID: 75806

In stock

Item Number

T432502

Grouped product items
SKU	Size	Availability	Price	Qty
T432502-100g	100g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$221.90
T432502-500g	500g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$772.90

Basic Description

Synonyms	34HJS55VCG \| C18H33P \| (Cy)3P \| Cy3P \| tri(cyclohexyl)phosphine \| tri-(cyclohexyl)phosphine \| Tri(cyclohexyl)-phosphine \| 2,3(or 3,4)-Dichlorobenzenemethanol methylcarbamate \| Phosphine, tricyclohexyl- \| Besuntol \| EINECS 220-069-2 \| P(Cy)3 \| PHOSPHATE SA
Specifications & Purity	20 wt. % in toluene
Product Description	Application Catalyst for: Carbonylative Suzuki-coupling of benzyl halides with potassium aryltrifluoroborates Suzuki-Miyaura reactions of aryl sulfonates / halides with arylboronic acids Synthesis of an acromelic acid A analog based 11C-labeled PET tracer Synthesis of (-)-Exiguolide and its analogues Allylation of zinc enolates Reagent used as a ligand for a range of metal-catalyzed organic transformations.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organophosphorus compounds
  - Class Organic phosphines and derivatives

Kingdom	Organic compounds
Superclass	Organophosphorus compounds
Class	Organic phosphines and derivatives
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Organic phosphines and derivatives
Alternative Parents	Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework	Aliphatic homomonocyclic compounds
Substituents	Phosphine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as organic phosphines and derivatives. These are organic compounds containing a phosphine derivative, with the general formula B1P(R2)R3 (R1-R3=alkyl, aryl).
External Descriptors	Not available
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

Names and Identifiers

IUPAC Name	tricyclohexylphosphane
INCHI	InChI=1S/C18H33P/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h16-18H,1-15H2
InChIKey	WLPUWLXVBWGYMZ-UHFFFAOYSA-N
Smiles	C1CCC(CC1)P(C2CCCCC2)C3CCCCC3
Isomeric SMILES	C1CCC(CC1)P(C2CCCCC2)C3CCCCC3
WGK Germany	3
PubChem CID	75806
Molecular Weight	280.43
Beilstein	957171

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Flash Point(°F)	48 °F
Flash Point(°C)	-20°C
Boil Point(°C)	110°C
Melt Point(°C)	77-83°C
Molecular Weight	280.400 g/mol
XLogP3	5.400
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	3
Exact Mass	280.232 Da
Monoisotopic Mass	280.232 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	19
Formal Charge	0
Complexity	202.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Zhinan Jiang, Yang Liu, Lina Ding, Yonggang Yang, Tiantian Guan, Chaochao Qin, Yufang Liu. (2024) Time-resolved excited-state dynamics of star-shaped carbazole-based room temperature phosphorescent molecule by ultrafast absorption spectroscopy. JOURNAL OF LUMINESCENCE, 266 (120275).
2. Yuanfei Bao, Jianliang Liu, Yige Zhang, Liping Zheng, Jiacong Ma, Fei Zhang, Yubing Xiong, Xiangju Meng, Zhifeng Dai, Feng-Shou Xiao. (2023) Porous organic polymers with diverse quaternary phosphonium units for chemical fixation of CO2 with low concentration. FUEL, 331 (125909).
3. Zhen-Jie Huang, Feng Li, Jia-Ping Xie, Hong-Rong Mou, Cheng-Bin Gong, Qian Tang. (2021) Electrochromic materials based on tetra-substituted viologen analogues with broad absorption and good cycling stability. SOLAR ENERGY MATERIALS AND SOLAR CELLS, 223 (110968).
4. Cheng Fang, Ma Xiaochun, Feng Qiancheng, Wang Hanqi, Yin Meng, He Wei. (2019) Preparation and characterization of DNA array slides via surface Michael addition. Biointerphases, 14 (6):
5. Fang Cheng, Hanqi Wang, Wei He, Bingbing Sun, Jing Zhao, Jingping Qu, Qing Wang. (2019) New Strategy for Functionalization of Silica Materials via Catalytic Oxa-Michael Reaction of Surface Silanol Groups with Vinyl Sulfones. ACS Sustainable Chemistry & Engineering, 7 (10): (9112–9120).
6. Yuan Chen, Wenqiang Tan, Qing Li, Fang Dong, Guodong Gu, Zhanyong Guo. (2018) Synthesis of inulin derivatives with quaternary phosphonium salts and their antifungal activity. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 113 (1273).

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