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2-(4-METHYLPHENYL)PYRROLIDINE, with the molecular formula C11H15N, is a pyrrolidine derivative featuring a 4-methylphenyl group attached to the pyrrolidine ring. 2-(4-METHYLPHENYL)PYRROLIDINE is known for its versatility in organic synthesis and pharmaceutical research, serving as a building block for synthesizing other organic compounds and as a starting material for pharmaceutical drug production. The 4-methylphenyl group contributes steric hindrance and hydrophobicity, which can significantly affect the compound's chemical and biological properties.

62506-76-7

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62506-76-7 Usage

Uses

Used in Organic Synthesis:
2-(4-METHYLPHENYL)PYRROLIDINE is used as a building block for the synthesis of other organic compounds, leveraging its structural features to create a variety of chemical entities.
Used in Pharmaceutical Research and Drug Development:
2-(4-METHYLPHENYL)PYRROLIDINE is used as a starting material in the production of pharmaceutical drugs, where its unique molecular structure can be harnessed to develop new therapeutic agents.
Used in the Chemical Industry:
2-(4-METHYLPHENYL)PYRROLIDINE is used to impart specific chemical and biological properties to molecules, such as steric hindrance and hydrophobicity, which can be crucial for the compound's performance in various chemical processes and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 62506-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,0 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62506-76:
(7*6)+(6*2)+(5*5)+(4*0)+(3*6)+(2*7)+(1*6)=117
117 % 10 = 7
So 62506-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H15N/c1-9-4-6-10(7-5-9)11-3-2-8-12-11/h4-7,11-12H,2-3,8H2,1H3

62506-76-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Methylphenyl)pyrrolidine

1.2 Other means of identification

Product number -
Other names 2-(4-METHYLPHENYL)PYRROLIDINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62506-76-7 SDS

62506-76-7Relevant academic research and scientific papers

O-benzoylhydroxylamines as alkyl nitrene precursors: Synthesis of saturated N-heterocycles from primary amines

Noda, Hidetoshi,Asada, Yasuko,Shibasaki, Masakatsu

, p. 8769 - 8773 (2020/10/12)

We introduce O-benzoylhydroxylamines as competent alkyl nitrene precursors. The combination of readily available, stable substrates and a proficient rhodium catalyst provides a straightforward means for the construction of various pyrrolidine rings from the corresponding primary amines. Preliminary mechanistic investigation suggests that the structure of the nitrene precursor plays a role in determining the nature of the resulting reactive intermediate.

Palladium-catalyzed ortho-olefination of 2-arylpyrrolidines: A tool for increasing structural complexity in nitrogen heterocycles

Legarda, Pablo D.,García-Rubia, Alfonso,Arrayás, Ramón Gómez,Carretero, Juan C.

, p. 3947 - 3954 (2018/06/11)

The dual role of the (2-pyridyl)sulfonyl unit as directing functionality and readily removable N-protecting group has enabled an efficient and practical transformation of 2-arylpyrrolidine derivatives into more complex tricyclic frameworks via palladium-catalyzed ortho-olefination with electron deficient alkenes and subsequent cyclization upon N-deprotection under mild conditions. The key cross coupling step in the presence of N-fluoro-2,4,6-trimethylpyridinium triflate ([F+]) as the terminal oxidant is both highly efficient and tolerant to a variety of steric and electronic changes at both coupling partners. By adequate choice of reductive conditions, the N-sulfonyl deprotection can be directed to the selective formation of benzo-fused pyrrolizidine or fused pyrrolidino-benzazapine frameworks.

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