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CAS

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928056-25-1

(S)-1-N-Benzyl-2-cyano-pyrrolidine, a chiral molecule with the molecular formula C13H14N2, is a derivative of pyrrolidine. It is characterized by its non-superimposable mirror image, making it a valuable building block in the synthesis of various pharmaceutical compounds. (S)-1-N-BENZYL-2-CYANO-PYRROLIDINE is instrumental in the preparation of enantiomerically pure compounds, which are essential for the production of drugs with specific biological activity in the pharmaceutical industry. Its role is pivotal in the development of new drugs and in the realm of organic chemical synthesis.

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  • 928056-25-1 Structure

  • Basic information

    1. Product Name: (S)-1-N-BENZYL-2-CYANO-PYRROLIDINE
    2. Synonyms: 2-Pyrrolidinecarbonitrile, 1-(phenylmethyl)-, (2S)-
    3. CAS NO:928056-25-1
    4. Molecular Formula: C12H14N2
    5. Molecular Weight: 186.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 928056-25-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 313.3°C at 760 mmHg
    3. Flash Point: 132.8°C
    4. Appearance: /
    5. Density: 1.08g/cm3
    6. Vapor Pressure: 0.0005mmHg at 25°C
    7. Refractive Index: 1.572
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (S)-1-N-BENZYL-2-CYANO-PYRROLIDINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: (S)-1-N-BENZYL-2-CYANO-PYRROLIDINE(928056-25-1)
    12. EPA Substance Registry System: (S)-1-N-BENZYL-2-CYANO-PYRROLIDINE(928056-25-1)

  • 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: 928056-25-1(Hazardous Substances Data)

928056-25-1 Usage

Uses

Used in Pharmaceutical Industry:
(S)-1-N-Benzyl-2-cyano-pyrrolidine is used as a key building block for the synthesis of pharmaceutical compounds. Its chiral nature allows for the creation of enantiomerically pure compounds, which are crucial for developing drugs with targeted biological activity and reduced side effects.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-1-N-benzyl-2-cyano-pyrrolidine serves as an important intermediate. Its unique structure facilitates the formation of complex organic molecules, contributing to the advancement of chemical research and the development of novel materials and compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 928056-25-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,0,5 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 928056-25:
(8*9)+(7*2)+(6*8)+(5*0)+(4*5)+(3*6)+(2*2)+(1*5)=181
181 % 10 = 1
So 928056-25-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2/c13-9-12-7-4-8-14(12)10-11-5-2-1-3-6-11/h1-3,5-6,12H,4,7-8,10H2/t12-/m0/s1

928056-25-1SDS

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 (2S)-1-benzylpyrrolidine-2-carbonitrile

1.2 Other means of identification

Product number -
Other names (S)-1-benzylpyrrolidine-2-carbonitrile

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:928056-25-1 SDS

928056-25-1Downstream Products

928056-25-1Relevant articles and documents

Strained azetidinium ylides: New reagents for cyclopropanation

Couty, Francois,David, Olivier,Larmanjat, Benedicte,Marrot, Jerome

, p. 1058 - 1061 (2008/02/05)

(Chemical Equation Presented) Azetidinium ylides showed a remarkable ability to perform the cyclopropanation of Michael acceptors. Ephedrine-derived azetidinium ylides allowed the formation of substituted cyclopropanes in good yields and at a high level o

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