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105849-94-3

Ethanone, 2-(5-methyl-1H-tetrazol-1-yl)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105849-94-3 Structure

  • Basic information

    1. Product Name: Ethanone, 2-(5-methyl-1H-tetrazol-1-yl)-1-phenyl-
    2. Synonyms:
    3. CAS NO:105849-94-3
    4. Molecular Formula: C10H10N4O
    5. Molecular Weight: 202.216
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105849-94-3.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: Ethanone, 2-(5-methyl-1H-tetrazol-1-yl)-1-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 2-(5-methyl-1H-tetrazol-1-yl)-1-phenyl-(105849-94-3)
    11. EPA Substance Registry System: Ethanone, 2-(5-methyl-1H-tetrazol-1-yl)-1-phenyl-(105849-94-3)

  • 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: 105849-94-3(Hazardous Substances Data)

105849-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105849-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,4 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105849-94:
(8*1)+(7*0)+(6*5)+(5*8)+(4*4)+(3*9)+(2*9)+(1*4)=143
143 % 10 = 3
So 105849-94-3 is a valid CAS Registry Number.

105849-94-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-Methyl-tetrazol-1-yl)-1-phenyl-ethanone

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:105849-94-3 SDS

105849-94-3Downstream Products

105849-94-3Relevant articles and documents

Phenyl oxime derivative and preparation method and application thereof

-

Paragraph 0137-0138, (2020/12/31)

The invention relates to a phenyl oxime derivative as well as a preparation method and application thereof. Specifically, the present invention relates to a phenyl oxime derivative represented by formula (I) or a stereoisomer of the phenyl oxime derivativ

Azido-Enolonium Species in C-C and C-N Bond-Forming Coupling Reactions

More, Atul A.,Santra, Sourav K.,Szpilman, Alex M.

supporting information, p. 768 - 771 (2020/01/31)

Vinyl azides react with boron trifluoride activated Koser's hypervalent iodine reagent to afford azido-enolonium species. These previously unknown azido-enolonium species react efficiently with aromatic compounds, allyltrimethylsilane, and azoles under mi

α-N-Heteroarylation and α-Azidation of Ketones via Enolonium Species

More, Atul A.,Pathe, Gulab K.,Parida, Keshaba N.,Maksymenko, Shimon,Lipisa, Yuriy B.,Szpilman, Alex M.

, p. 2442 - 2447 (2018/02/23)

Enolonium species, resulting from the umpolung of ketone enolates by Koser's hypervalent iodine reagents activated by boron trifluoride, react with a variety of nitrogen heterocycles to form α-aminated ketones. The reactions are mild and complete in 4-5 h. Additionally, α-azidation of the enolonium species takes place using trimethylsilyl azide as a convenient source of azide nucleophile.

Synthesis and Properties of Tetrazolium N-Phenacylides

Moderhack, Dietrich,Lembcke, Adalbert

, p. 1157 - 1164 (2007/10/02)

A number of isomeric tetrazolium 1-phenacylides (6) and 3-phenacylides (7) have been prepared by deprotonation of the corresponding salts (3) and (4) and submitted the standard ylide reactions.A comparison of their physicochemical pr

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