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(S)-1-Benzyl-3-N-BOC-aminomethylpyrrolidine is a chiral amine compound characterized by the presence of a benzyl group attached to the nitrogen atom and a BOC (tert-butoxycarbonyl) protecting group on the amino group. It belongs to the class of amines and is recognized for its reactivity and ability to participate in various organic reactions. The unique structure and chirality of (S)-1-BENZYL-3-N-BOC-AMINOMETHYLPYRROLIDINE make it an important intermediate in the synthesis of biologically active molecules and pharmaceuticals, contributing to its value in the chemical and pharmaceutical industries.

303111-41-3

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303111-41-3 Usage

Uses

Used in Organic Synthesis:
(S)-1-Benzyl-3-N-BOC-aminomethylpyrrolidine is used as a key intermediate in organic synthesis for its ability to create diverse molecules. Its reactivity allows it to participate in a wide range of organic reactions, making it a valuable component in the development of new chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (S)-1-Benzyl-3-N-BOC-aminomethylpyrrolidine is utilized as a building block for the synthesis of biologically active molecules. Its chiral nature and unique structure enable the creation of enantiomerically pure compounds, which are essential for the development of effective and selective drugs.
Used in the Synthesis of Biologically Active Molecules:
(S)-1-Benzyl-3-N-BOC-aminomethylpyrrolidine is employed as a precursor in the synthesis of biologically active molecules due to its potential to form various molecular structures. Its versatility in organic reactions facilitates the production of compounds with specific biological activities, contributing to advancements in medicinal chemistry.
Used in the Development of Enantiomerically Pure Compounds:
Owing to its chiral properties, (S)-1-Benzyl-3-N-BOC-aminomethylpyrrolidine is used in the development of enantiomerically pure compounds, which are crucial for the pharmaceutical industry. The ability to produce such compounds ensures that drugs exhibit the desired therapeutic effects with minimal side effects, improving patient outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 303111-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,3,1,1 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 303111-41:
(8*3)+(7*0)+(6*3)+(5*1)+(4*1)+(3*1)+(2*4)+(1*1)=63
63 % 10 = 3
So 303111-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H26N2O2/c1-17(2,3)21-16(20)18-11-15-9-10-19(13-15)12-14-7-5-4-6-8-14/h4-8,15H,9-13H2,1-3H3,(H,18,20)/t15-/m0/s1

303111-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[[(3S)-1-benzylpyrrolidin-3-yl]methyl]carbamate

1.2 Other means of identification

Product number -
Other names -

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:303111-41-3 SDS

303111-41-3Relevant academic research and scientific papers

QUINOLONE ANTIBACTERIAL AGENTS

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Page/Page column 87; 88; 121, (2010/02/12)

Compounds of formula (I) wherein A is formula (II), formula (III) or formula (IV), and B is formula (V), formula (VI), or formula (VII), can be used in a variety of applications including use as antibacterial agents.

ANTIBACTERIAL AMINOQUINAZOLIDINEDIONE DERIVATIVES

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Page/Page column 115; 116; 149, (2010/02/12)

Compounds of formula (I) wherein: A is Formula (II), Formula (III), or Formula (IV) and B is Formula (V), Formula (VI), or Formula (VII), can be used in a variety of applications including use as antibacterial agents.

Phenyloxazoles and phenylthiazoles as benzamide bioisosteres: Synthesis and dopamine receptor binding profiles

Einsiedel, Juergen,Thomas, Christoph,Huebner, Harald,Gmeiner, Peter

, p. 2041 - 2044 (2007/10/03)

Conformationally restricted benzamide bioisosteres were investigated when the aminomethylpyrrolidine derivative 4o proved D3 as well as D4 binding properties which were comparable to those of the atypical neuroleptics sulpiride and clozapine, respectively. (C) 2000 Elsevier Science Ltd.

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