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847548-23-6

2-Azetidinone, 3-bromo-3-(1E)-1-butenyl-4-phenyl-1-[(1S)-1-phenylethyl]-, (3S,4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 847548-23-6 Structure

  • Basic information

    1. Product Name: 2-Azetidinone, 3-bromo-3-(1E)-1-butenyl-4-phenyl-1-[(1S)-1-phenylethyl]-, (3S,4R)-
    2. Synonyms:
    3. CAS NO:847548-23-6
    4. Molecular Formula: C21H22BrNO
    5. Molecular Weight: 384.316
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 847548-23-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Azetidinone, 3-bromo-3-(1E)-1-butenyl-4-phenyl-1-[(1S)-1-phenylethyl]-, (3S,4R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Azetidinone, 3-bromo-3-(1E)-1-butenyl-4-phenyl-1-[(1S)-1-phenylethyl]-, (3S,4R)-(847548-23-6)
    11. EPA Substance Registry System: 2-Azetidinone, 3-bromo-3-(1E)-1-butenyl-4-phenyl-1-[(1S)-1-phenylethyl]-, (3S,4R)-(847548-23-6)

  • 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: 847548-23-6(Hazardous Substances Data)

847548-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 847548-23-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,5,4 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 847548-23:
(8*8)+(7*4)+(6*7)+(5*5)+(4*4)+(3*8)+(2*2)+(1*3)=206
206 % 10 = 6
So 847548-23-6 is a valid CAS Registry Number.

847548-23-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S',3S,4R)-3-bromo-3-but-1-enyl-4-phenyl-1-(1-phenylethyl)azetidin-2-one

1.2 Other means of identification

Product number -
Other names (3S,4R)-3-Bromo-3-((E)-but-1-enyl)-4-phenyl-1-((S)-1-phenyl-ethyl)-azetidin-2-one

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:847548-23-6 SDS

847548-23-6Relevant articles and documents

Highly diastereoselective allylic azide formation and isomerization. Synthesis of 3(2′-amino)-β-lactams

Cardillo, Giuliana,Fabbroni, Serena,Gentilucci, Luca,Perciaccante, Rossana,Piccinelli, Fabio,Tolomelli, Alessandra

, p. 533 - 536 (2007/10/03)

(Chemical Equation Presented) The stereoselective anti S N2′ attack of NaN3 to 3-alkenyl-3-bromo-azetidin-2- ones gave a mixture of diastereomeric azides in fast equilibrium. The [3,3]-sigmatropic rearrangement of allylic azides occu

Zinc metal-promoted nucleophilic addition of azetidin-2-ones to aldehydes and nitriles

Benfatti, Fides,Cardillo, Giuliana,Fabbroni, Serena,Gentilucci, Luca,Perciaccante, Rossana,Piccinelli, Fabio,Tolomelli, Alessandra

, p. 61 - 70 (2007/10/03)

The reactivity of in situ generated organozinc reagents of 3-alkenyl-3-bromoazetidin-2-ones with aromatic and aliphatic aldehydes to give the corresponding alcohol derivatives has been studied. The effect of solvent and Lewis acids has been explored in or

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