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874279-33-1

Quinoxaline, 6-ethenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 874279-33-1 Structure

  • Basic information

    1. Product Name: Quinoxaline, 6-ethenyl-
    2. Synonyms: Quinoxaline, 6-ethenyl-
    3. CAS NO:874279-33-1
    4. Molecular Formula: C10H8N2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 874279-33-1.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Quinoxaline, 6-ethenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Quinoxaline, 6-ethenyl-(874279-33-1)
    11. EPA Substance Registry System: Quinoxaline, 6-ethenyl-(874279-33-1)

  • 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: 874279-33-1(Hazardous Substances Data)

874279-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 874279-33-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,2,7 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 874279-33:
(8*8)+(7*7)+(6*4)+(5*2)+(4*7)+(3*9)+(2*3)+(1*3)=211
211 % 10 = 1
So 874279-33-1 is a valid CAS Registry Number.

874279-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-ethenylquinoxaline

1.2 Other means of identification

Product number -
Other names 6-vinylquinoxaline

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:874279-33-1 SDS

874279-33-1Relevant articles and documents

Nickel-Catalyzed Ligand-Free Hiyama Coupling of Aryl Bromides and Vinyltrimethoxysilane

Wei, Shichao,Mao, Yongjun,Shi, Shi-Liang

supporting information, p. 1670 - 1674 (2021/02/26)

We herein disclose the first Ni-catalyzed Hiyama coupling of aryl halides with vinylsilanes. This protocol uses cheap, nontoxic, and stable vinyltrimethoxysilane as the vinyl donor, proceeds under mild and ligand-free conditions, furnishing a diverse variety of styrene derivatives in high yields with excellent functional group compatibility.

Superacid-promoted additions involving vinyl-substituted pyrimidines, quinoxalines, and quinazolines: Mechanisms correlated to charge distributions

Zhang, Yiliang,Sheets, Matthew R.,Raja, Erum K.,Boblak, Kenneth N.,Klumpp, Douglas A.

supporting information; experimental part, p. 8467 - 8469 (2011/07/29)

The superacid-promoted reactions of vinyl-substituted N-heterocycles have been studied. Diprotonated pyrimidines, quinoxalines, and quinazolines exhibit an unusual regioelectronic effect that controls the type of addition reaction observed. Depending on the ring position of the vinyl substituent, either conjugate addition or Markovnikov addition occurs. The mode of addition has been shown to correlate well to NBO calculated charges.

Identification of 2-(4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-3-yl)-ethylamine derivatives as novel GnRH receptor antagonists

Chen, Mi,Guo, Zhiqiang,Lanier, Marion C.,Zhao, Liren,Betz, Stephen F.,Huang, Charles Q.,Loweth, Colin J.,Ashweek, Neil J.,Liu, Xin-Jun,Struthers, R. Scott,Bradbury, Margaret J.,Behan, James W.,Wen, Jenny,O'Brien, Zhihong,Saunders, John,Zhu, Yun-Fei

, p. 3845 - 3850 (2008/02/13)

A novel series of 2-(4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-3-yl)-ethylamine derivatives were designed and synthesized as GnRH receptor antagonists. SAR studies led to a series of highly active molecules against both the rat and human receptors. Furt

Piperazinylimidazopyridine and piperazinyltriazolopyridine antagonists of gonadotropin releasing hormone receptor

-

Page/Page column 37, (2008/06/13)

The present invention relates to Gonadotropin Releasing Hormone (GnRH, also known as Luteinizing Hormone Releasing Hormone) receptor antagonists.

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