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6317-35-7

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6317-35-7 Usage

General Description

Ethyl pyrrolidine-1-propionate is a chemical compound with a molecular formula C9H17NO2. It belongs to the family of pyrrolidine derivatives and is commonly used as a flavoring agent in the food and beverage industry. It is also known for its potential medicinal properties, including its use in the synthesis of pharmaceutical drugs. Ethyl pyrrolidine-1-propionate is a colorless and odorless liquid with a slightly sweet taste. It is considered safe for consumption in small quantities, but excessive exposure to the compound may lead to health concerns. Overall, it is a versatile chemical with applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6317-35-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6317-35:
(6*6)+(5*3)+(4*1)+(3*7)+(2*3)+(1*5)=87
87 % 10 = 7
So 6317-35-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO2/c1-2-12-9(11)5-8-10-6-3-4-7-10/h2-8H2,1H3

6317-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3-pyrrolidin-1-ylpropanoate

1.2 Other means of identification

Product number -
Other names ethyl 3-tetrahydro-1H-1-pyrrolilpropanoate

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:6317-35-7 SDS

6317-35-7Relevant articles and documents

Ir-catalyzed chemoselective reduction of β-amido esters: A versatile approach to β-enamino esters

Yang, Zhi-Ping,Lu, Guang-Sheng,Ye, Jian-Liang,Huang, Pei-Qiang

, p. 1624 - 1631 (2019/01/04)

The conversion of β-amido esters to β-enamino esters is an indispensable step for some synthetic approaches to alkaloids and related medicines. Known methods for such transformation are not only stepwise, but also proceed with low atom-efficiency. Herein, we report a direct and versatile approach that features the Ir-catalyzed chemoselective reduction of β-amido esters with 1,1,3,3-tetramethyldisiloxane (TMDS). In addition, a lack of some signals was observed in the 13C NMR spectra of some alicyclic β-enamino esters. This revealed a longstanding existing but being ignored phenomenon in the literature.

N-Acylaminophenothiazines: Neuroprotective agents displaying multifunctional activities for a potential treatment of Alzheimer's disease

González-Mu?oz, Gema C.,Arce, Mariana P.,López, Beatriz,Pérez, Concepción,Romero, Alejandro,Barrio, Laura Del,Martín-De-Saavedra, María Dolores,Egea, Javier,León, Rafael,Villarroya, Mercedes,López, Manuela G.,García, Antonio G.,Conde, Santiago,Rodríguez-Franco, María Isabel

body text, p. 2224 - 2235 (2011/06/22)

We have previously reported the multifunctional profile of N-(3-chloro-10H-phenothiazin-10-yl)-3-(dimethylamino)propanamide (1) as an effective neuroprotectant and selective butyrylcholinesterase inhibitor. In this paper, we have developed a series of N-acylaminophenothiazines obtained from our compound library or newly synthesised. At micro- and sub-micromolar concentrations, these compounds selectively inhibited butyrylcholinesterase (BuChE), protected neurons against damage caused by both exogenous and mitochondrial free radicals, showed low toxicity, and could penetrate into the CNS. In addition, N-(3-chloro-10H-phenothiazin-10-yl)-2-(pyrrolidin-1-yl) acetamide (11) modulated the cytosolic calcium concentration and protected human neuroblastoma cells against several toxics, such as calcium overload induced by an l-type Ca2+-channel agonist, tau-hyperphosphorylation induced by okadaic acid and Aβ peptide.

Samarium(III) triflate catalyzed conjugate addition of amines to electron-deficient alkenes

Yadav,Ramesh Reddy,Gopal Rao,Narsaiah,Subba Reddy

, p. 3447 - 3450 (2008/09/19)

Amines undergo smooth nucleophilic addition to α,β-unsaturated compounds in the presence of a catalytic amount of samarium(III) triflate at ambient temperature to produce the corresponding β-amino compounds in excellent yields. This method is simple, convenient, and works efficiently under mild conditions. Georg Thieme Verlag Stuttgart.

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