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349426-35-3

N-(3-bromophenyl)cinnamamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 349426-35-3 Structure

  • Basic information

    1. Product Name: N-(3-bromophenyl)cinnamamide
    2. Synonyms:
    3. CAS NO:349426-35-3
    4. Molecular Formula:
    5. Molecular Weight: 302.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 349426-35-3.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: N-(3-bromophenyl)cinnamamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(3-bromophenyl)cinnamamide(349426-35-3)
    11. EPA Substance Registry System: N-(3-bromophenyl)cinnamamide(349426-35-3)

  • 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: 349426-35-3(Hazardous Substances Data)

349426-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 349426-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,9,4,2 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 349426-35:
(8*3)+(7*4)+(6*9)+(5*4)+(4*2)+(3*6)+(2*3)+(1*5)=163
163 % 10 = 3
So 349426-35-3 is a valid CAS Registry Number.

349426-35-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-bromophenyl)cinnamamide

1.2 Other means of identification

Product number -
Other names -

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:349426-35-3 SDS

349426-35-3Relevant articles and documents

DDQ-promoted direct transformation of benzyl hydrocarbons to amides via tandem reaction of the CDC reaction and Beckmann rearrangement

Qiu, Jun,Zhang, Ronghua

supporting information, p. 6008 - 6012 (2013/09/12)

An atom-efficient and transition metal-free approach to amides from the corresponding benzyl hydrocarbons through C-H and C-C bond cleavage has been developed. Mechanistic studies have shown that a DDQ-promoted cross-dehydrogenative coupling (CDC) reaction with subsequent oxidation and rearrangement are involved in this transformation. The Royal Society of Chemistry.

Synthesis, SAR and in vivo activity of novel thienopyridine sulfonamide pyrrolidinones as factor Xa inhibitors

Becker, Michael R.,Ewing, William R.,Davis, Roderick S.,Pauls, Henry W.,Ly, Cuong,Li, Aiwen,Mason, Helen J.,Choi-Sledeski, Yong Mi,Spada, Alfred P.,Chu, Valeria,Brown, Karen D.,Colussi, Dennis J.,Leadley, Robert J.,Bentley, Ross,Bostwick, Jeff,Kasiewski, Charles,Morgan, Suzanne

, p. 2753 - 2758 (2007/10/03)

Thienopyridine sulfonamide pyrrolidinones were found to be potent and selective inhibitors of the coagulation cascade enzyme factor Xa. SAR studies led to several compounds that were selected for further in vivo investigation. These novel aryl binding pocket moieties represent a structural modification to a series of fXa inhibitors. Several compounds proved to be efficacious iv antithrombotic agents.

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