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(3R,4R)-1-[(tert-butoxy)carbonyl]-4-(ethoxycarbonyl)pyrrolidineis a pyrrolidine derivative with the molecular formula C12H23NO4. It contains both a tert-butoxycarbonyl and an ethoxycarbonyl group, making it a versatile compound for various applications in organic synthesis, drug development, and medicinal chemistry.

595556-31-3

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595556-31-3 Usage

Uses

Used in Organic Synthesis:
(3R,4R)-1-[(tert-butoxy)carbonyl]-4-(ethoxycarbonyl)pyrrolidineis used as a building block for the synthesis of complex organic compounds. The presence of the tert-butoxycarbonyl and ethoxycarbonyl groups allows for further functionalization and modification of the molecule, enabling the creation of a wide range of organic compounds.
Used in Drug Development:
(3R,4R)-1-[(tert-butoxy)carbonyl]-4-(ethoxycarbonyl)pyrrolidineis used as a key intermediate in the development of new pharmaceuticals. Its unique structure and functional groups make it a promising candidate for the synthesis of bioactive molecules with potential therapeutic applications.
Used in Medicinal Chemistry:
(3R,4R)-1-[(tert-butoxy)carbonyl]-4-(ethoxycarbonyl)pyrrolidineis used as a chiral auxiliary in asymmetric synthesis, facilitating the production of enantiomerically pure compounds. This is particularly important in medicinal chemistry, where the stereochemistry of a molecule can significantly impact its biological activity and safety profile.
Further research and experimentation may reveal additional potential uses and properties of (3R,4R)-1-[(tert-butoxy)carbonyl]-4-(ethoxycarbonyl)pyrrolidine-, expanding its applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 595556-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,5,5,5 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 595556-31:
(8*5)+(7*9)+(6*5)+(5*5)+(4*5)+(3*6)+(2*3)+(1*1)=203
203 % 10 = 3
So 595556-31-3 is a valid CAS Registry Number.

595556-31-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R,4R)-4-(Ethoxycarbonyl)-1-{[(2-methyl-2-propanyl)oxy]carbonyl} -3-pyrrolidinecarboxylic acid

1.2 Other means of identification

Product number -
Other names (3R,4R)-trans-N-Boc-pyrrolidine-3,4-dicarboxylic acid monoethyl ester

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:595556-31-3 SDS

595556-31-3Relevant academic research and scientific papers

TRIAZOLE-ISOXAZOLE COMPOUND AND MEDICAL USE THEREOF

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Paragraph 3312; 3313, (2016/06/06)

A compound represented by Formula [I]: or pharmaceutically acceptable salt thereof, wherein each symbol is as defined in the description.

NEW SOLID FORMS OF FXA INHIBITORS

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, (2009/01/20)

The invention is concerned with crystalline forms or amorphous forms of a pyrrolidine- 3,4-dicarboxamide derivative, which is useful as an active ingredient of medicaments for the diseases which can be treated by the coagulation factor Xa inhibitors.

PROCESSES FOR THE PREPARATION OF (3R, 4R) -N- (4 -CHLOROPHENYL) -1- (2, 2-DIFLUOROETHYL) -N' - [2-FLUORO-4- (2-OXO-1 (2H) -PYRIDINYL) PHENYL] -3, 4-PYRROLIDINEDICARBOXAMIDE

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Page/Page column 30, (2008/12/06)

The invention is concerned with processes for the manufacture of pyrrolidine-3,4- dicarboxamide derivative of formula (I), and the intermediates useful for those processes.

NOVEL PYRROLIDINE-3,4-DICARBOXAMIDE DERIVATIVES

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Page/Page column 33; 39-40; 43, (2008/06/13)

The invention is concerned with novel pyrrolidine-3,4-dicarboxamide derivatives of Formula (I) ; wherein Rl to R9 and X are as defined in the description and in the claims, as well as physiologically acceptable salts thereof. These c

Chemoenzymatic preparation of non-racemic N-Boc-pyrrolidine-3,4-dicarboxylic acid 3-ethyl esters and their 4-hydroxymethyl derivatives

Rodriguez Sarmiento, Rosa Maria,Wirz, Beat,Iding, Hans

, p. 1547 - 1551 (2007/10/03)

For the synthesis of metalloproteinase inhibitors the (R,R)- and (S,S)-monoethyl esters of N-Boc-pyrrolidine-3,4-dicarboxylic acid were prepared as key intermediates from the trans-diester racemate by two consecutive, highly selective enzymatic reactions.

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