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170123-25-8

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170123-25-8 Usage

General Description

Ethyl N-Boc-3-oxopyrrolidine-2-carboxylate is a chemical compound that falls under the category of pharmaceutical intermediates, implying that it plays a crucial role in the production of pharmaceutical drugs. Characteristics of this chemical include its molecular formula of C11H17NO5 and a molecular weight of 243.257 g/mol. It is often used in the synthesis of several organic compounds due to its complex structured design. Furthermore, proper handling and usage of this substance are vital due to potential hazards. Detailed information about its properties, safety measures, and potential health effects can usually be found in its Material Safety Data Sheet (MSDS).

Check Digit Verification of cas no

The CAS Registry Mumber 170123-25-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,1,2 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 170123-25:
(8*1)+(7*7)+(6*0)+(5*1)+(4*2)+(3*3)+(2*2)+(1*5)=88
88 % 10 = 8
So 170123-25-8 is a valid CAS Registry Number.

170123-25-8SDS

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 3-Oxo-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

1.2 Other means of identification

Product number -
Other names 1-tert-butyl 2-ethyl 3-oxopyrrolidine-1,2-dicarboxylate

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:170123-25-8 SDS

170123-25-8Relevant articles and documents

Synthesis of (±)-acetylnorloline via stereoselective tethered aminohydroxylation

Hovey, M. Todd,Eklund, Emily J.,Pike, Robert D.,Mainkar, Anshul A.,Scheerer, Jonathan R.

, p. 1246 - 1249 (2011)

Loline alkaloids exhibit a strained ether-bridged pyrrolizidine skeleton and possess insecticidal and insect antifeedant properties. The synthesis of acetylnorloline, a prototypical member of the alkaloid family, is described. Central to the route is a st

Improved biomimetic total synthesis of D,L-stephacidin A

Greshock, Thomas J.,Williams, Robert M.

, p. 4255 - 4258 (2007)

The direct conversion of β-hydroxyproline derivatives into 5-hydroxypyrazin-2(1H)-ones under Mitsunobu conditions has been discovered to be a general biomimetic protocol generating IMDA intermediates and has been applied to the concise, biomimetic total syntheses of D,Lstephacldin A and D,L-brevianamide B.

Synthesis of models of the BC ring systems of MPC1001 and MPC1001F

Dong, Shuai,Indukuri, Kiran,Clive, Derrick L. J.,Gao, Jin-Ming

supporting information, p. 8271 - 8274 (2016/07/06)

Piperazinedione 13, representing the BC rings of the anti-prostate cancer fungal metabolite MPC1001, was prepared by a route in which a sulfur-stabilized carbanion derived from 22 cyclizes onto the terminal ester of the pendant chain attached to N1. Another model, 14, was synthesized by cyclization of an α-ketoamide nitrogen onto an ester; 14 represents the BC rings of MPC1001F.

Design and synthesis of 3-arylpyrrolidine-2-carboxamide derivatives as melanocortin-4 receptor ligands

Tran, Joe A.,Tucci, Fabio C.,Arellano, Melissa,Jiang, Wanlong,Chen, Caroline W.,Marinkovic, Dragan,Fleck, Beth A.,Wen, Jenny,Foster, Alan C.,Chen, Chen

, p. 1931 - 1938 (2008/09/20)

Based on 3-phenylpropionamides, a series of 3-arylpyrrolidine-2-carboxamide derivatives was designed and synthesized to study the effect of cyclizations as melanocortin-4 receptor ligands. It was found that the 2R,3R-pyrrolidine isomer possessed the most

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