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Pyrrolidine, 1-[(4-bromophenyl)azo]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 147227-33-6 Structure
  • Basic information

    1. Product Name: Pyrrolidine, 1-[(4-bromophenyl)azo]-
    2. Synonyms:
    3. CAS NO:147227-33-6
    4. Molecular Formula: C10H12BrN3
    5. Molecular Weight: 254.129
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 147227-33-6.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: Pyrrolidine, 1-[(4-bromophenyl)azo]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyrrolidine, 1-[(4-bromophenyl)azo]-(147227-33-6)
    11. EPA Substance Registry System: Pyrrolidine, 1-[(4-bromophenyl)azo]-(147227-33-6)
  • 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: 147227-33-6(Hazardous Substances Data)

147227-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147227-33-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,2 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 147227-33:
(8*1)+(7*4)+(6*7)+(5*2)+(4*2)+(3*7)+(2*3)+(1*3)=126
126 % 10 = 6
So 147227-33-6 is a valid CAS Registry Number.

147227-33-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-bromophenyl)-pyrrolidin-1-yldiazene

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:147227-33-6 SDS

147227-33-6Relevant articles and documents

Sulfide synthesis through copper-catalyzed C-S bond formation under biomolecule-compatible conditions

Zhang, Yonghong,Li, Yiming,Zhang, Xiaomei,Jiang, Xuefeng

supporting information, p. 941 - 944 (2015/01/09)

We report here an efficient and mild method for constructing C-S bonds. The reactions were carried out with Na2S2O3 as a sulfurating reagent, CuSO4 as a catalyst, and water as solvent without any surfactant. The products were achieved in moderate to excellent yields at room temperature under air. Notably, this reaction is compatible with various biomolecules including amino acids, oligosaccharides, nucleosides, proteins, and cell lysates. This journal is

COMPOSITIONS USEFUL FOR TREATING DISORDERS RELATED TO KIT

-

Paragraph 0227; 0228, (2015/04/28)

Compounds and compositions useful for treating disorders related to KIT and PDFGR are described herein.

Suzuki-Miyaura cross-coupling reaction of 1-aryltriazenes with arylboronic acids catalyzed by a recyclable polymer-supported N-heterocyclic carbene-palladium complex catalyst

Nan, Guangming,Ren, Fang,Luo, Meiming

experimental part, (2010/11/21)

The Suzuki-Miyaura cross-coupling reaction of 1-aryltriazenes with arylboronic acids catalyzed by a recyclable polymer-supported Pd-NHC complex catalyst has been realized for the first time. The polymer-supported catalyst can be re-used several times still retaining high activity for this transformation. Various aryltriazenes were investigated as electrophilic substrates at room temperature to give biaryls in good to excellent yields and showed good chemoselectivity over aryl halides in the reactions.

Synthesis and radiosynthesis of 17α -[p-(iodophenylethynyl)]estra-3,17β-diols

Wang, Jian,Watanabe, Masataka,Mataka, Shuntaro,Thiemann, Thies,Ribeiro Morais, Goreti,Roleira, Fernanda,Da Silva, Elisiario Tavares,Melo E Silva, Cristina

, p. 799 - 804 (2007/10/03)

Estrones have been subjected to an addition reaction with [(4-ethynylphenyl)azo]pyrrolidine to provide 17 α -{4-[(pyrrolidin-1-yl)-azo]phenylethynyl}estra-3,17 β-diols. A subsequent iodination with iodotrimethylsilane, produced in situ from chlorotrimethy

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