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1251570-77-0

(S)-tert-butyl 3-(3-methylbutanoyl)pyrrolidine-1-carboxylate is a pyrrolidine carboxylate chemical compound, characterized by a tert-butyl group attached to the nitrogen atom and a 3-methylbutanoyl group attached to the carbon atom. As a derivative of pyrrolidine carboxylic acid, it holds potential in the pharmaceutical industry and organic synthesis due to its unique stereochemistry and molecular structure.

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  • 1251570-77-0 Structure

  • Basic information

    1. Product Name: (S)-tert-butyl 3-(3-methylbutanoyl)pyrrolidine-1-carboxylate
    2. Synonyms: (S)-tert-butyl 3-(3-methylbutanoyl)pyrrolidine-1-carboxylate;(S)-1-Boc-3-(3-Methylbutanoyl)pyrrolidine
    3. CAS NO:1251570-77-0
    4. Molecular Formula: C14H25NO3
    5. Molecular Weight: 255
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1251570-77-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-tert-butyl 3-(3-methylbutanoyl)pyrrolidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-tert-butyl 3-(3-methylbutanoyl)pyrrolidine-1-carboxylate(1251570-77-0)
    11. EPA Substance Registry System: (S)-tert-butyl 3-(3-methylbutanoyl)pyrrolidine-1-carboxylate(1251570-77-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1251570-77-0(Hazardous Substances Data)

1251570-77-0 Usage

Uses

Used in Pharmaceutical Industry:
(S)-tert-butyl 3-(3-methylbutanoyl)pyrrolidine-1-carboxylate is used as a precursor for the synthesis of various bioactive molecules, leveraging its unique structural features to contribute to the development of new pharmaceutical agents.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-tert-butyl 3-(3-methylbutanoyl)pyrrolidine-1-carboxylate serves as a valuable building block for the preparation of complex molecules, facilitating the creation of intricate chemical structures for a range of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1251570-77-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,1,5,7 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1251570-77:
(9*1)+(8*2)+(7*5)+(6*1)+(5*5)+(4*7)+(3*0)+(2*7)+(1*7)=140
140 % 10 = 0
So 1251570-77-0 is a valid CAS Registry Number.

1251570-77-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (3S)-3-(3-methylbutanoyl)pyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names (S)-1-Boc-3-(3-methylbutanoyl)pyrrolidine

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:1251570-77-0 SDS

1251570-77-0Relevant articles and documents

Discovery of a potent, dual serotonin and norepinephrine reuptake inhibitor

Dreyfus, Nicolas,Myers, Jason K.,Badescu, Valentina O.,De Frutos, Oscar,De La Puente, Maria Luz,Ding, Chunjin,Filla, Sandra A.,Fynboe, Karsten,Gernert, Douglas L.,Heinz, Beverly A.,Hemrick-Luecke, Susan K.,Johnson, Kirk W.,Johnson, Michael P.,Lopez, Pilar,Love, Patrick L.,Martin, Laura J.,Masquelin, Thierry,McCoy, Michael J.,Mendiola, Javier,Morrow, Denise,Muhlhauser, Mark,Pascual, Gustavo,Perun, Thomas J.,Pfeifer, Lance A.,Phebus, Lee A.,Richards, Simon J.,Rincon, Juan Antonio,Seest, Eric P.,Shah, Jikesh,Shaojuan, Jia,Simmons, Rosa Maria A.,Stephenson, Gregory A.,Tromiczak, Eric G.,Thompson, Linda K.,Walter, Magnus W.,Weber, Wayne W.,Zarrinmayeh, Hamideh,Thomas, Craig E.,Joshi, Elizabeth,Iyengar, Smriti,Johansson, Anette M.

, p. 560 - 564 (2013/07/26)

The objective of the described research effort was to identify a novel serotonin and norepinephrine reuptake inhibitor (SNRI) with improved norepinephrine transporter activity and acceptable metabolic stability and exhibiting minimal drug-drug interaction. We describe herein the discovery of a series of 3-substituted pyrrolidines, exemplified by compound 1. Compound 1 is a selective SNRI in vitro and in vivo, has favorable ADME properties, and retains inhibitory activity in the formalin model of pain behavior. Compound 1 thus represents a potential new probe to explore utility of SNRIs in central nervous system disorders, including chronic pain conditions.

SEROTONIN AND NOREPINEPHRINE REUPTAKE INHIBITOR

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Page/Page column 5-6, (2010/11/03)

A serotonin and norepinephrine reuptake inhibitor of the formula: its uses, and methods for its preparation are described.

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