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129414-26-2

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129414-26-2 Usage

General Description

METHYL 4-PYRROLIDIN-1-YLBENZOATE is a chemical compound with the molecular formula C15H19NO2. It is a derivative of benzoic acid and contains a pyrrolidine group. METHYL 4-PYRROLIDIN-1-YLBENZOATE is commonly used in the production of pharmaceuticals, pesticides, and other organic compounds. It has a variety of industrial applications due to its ability to act as a building block for more complex molecules. Additionally, it has been studied for its potential biological and pharmacological properties, making it a subject of interest in the scientific community.

Check Digit Verification of cas no

The CAS Registry Mumber 129414-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,4,1 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129414-26:
(8*1)+(7*2)+(6*9)+(5*4)+(4*1)+(3*4)+(2*2)+(1*6)=122
122 % 10 = 2
So 129414-26-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO2/c1-15-12(14)10-4-6-11(7-5-10)13-8-2-3-9-13/h4-7H,2-3,8-9H2,1H3

129414-26-2SDS

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 Methyl 4-(1-pyrrolidinyl)benzenecarboxylate

1.2 Other means of identification

Product number -
Other names METHYL 4-PYRROLIDIN-1-YLBENZOATE

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:129414-26-2 SDS

129414-26-2Relevant articles and documents

Modular, Self-Assembling Metallaphotocatalyst for Cross-Couplings Using the Full Visible-Light Spectrum

Reischauer, Susanne,Strauss, Volker,Pieber, Bartholom?us

, p. 13269 - 13274 (2020)

The combination of nickel and photocatalysis has unlocked a variety of cross-couplings. These protocols rely on a few photocatalysts that can only convert a small portion of visible light (500 nm) into chemical energy. The high-energy photons that excite

Ad Hoc Adjustment of Photoredox Properties by the Late-Stage Diversification of Acridinium Photocatalysts

Hutskalova, Valeriia,Sparr, Christof

supporting information, p. 5143 - 5147 (2021/06/30)

The steadily growing interest in substituting precious-metal photoredox catalysts with organic surrogates is vibrantly sustained by emerging methodologies to vary their photochemical behavior. Herein, we report an ad hoc approach for the preparation of acridinium salts with a particularly broad range of photoredox properties. The method involves an aryne-imine-aryne coupling to a linchpin tetrafluoro acridinium salt for a late-stage diversification by nucleophilic aromatic substitution reactions to form diaminoacridinium and undescribed aza-rhodol photocatalysts. The different functionalities and redox properties of the organic acridinium photocatalysts render them suitable for bifunctional photoredox catalysis and organocatalytic photochemical C-N cross-couplings.

Organic photoredox catalytic α-C(sp3)-H phosphorylation of saturated: Aza -heterocycles

Yi, Ming-Jun,Xiao, Teng-Fei,Li, Wen-Hui,Zhang, Yi-Fan,Yan, Pen-Ji,Zhang, Baoxin,Xu, Peng-Fei,Xu, Guo-Qiang

supporting information, p. 13158 - 13161 (2021/12/16)

A metal-free C(sp3)-H phosphorylation of saturated aza-heterocycles via the merger of organic photoredox and Br?nsted acid catalyses was established under mild conditions. This protocol provided straightforward and economic access to a variety of valuable α-phosphoryl cyclic amines by using commercially available diarylphosphine oxide reagents. In addition, the D-A fluorescent molecule DCQ was used for the first time as a photocatalyst and exhibited an excellent photoredox catalytic efficiency in this transformation. A series of mechanistic experiments and DFT calculations demonstrated that this transformation underwent a sequential visible light photoredox catalytic oxidation/nucleophilic addition process.

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