Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1696-17-9

Post Buying Request

1696-17-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1696-17-9 Usage

Uses

N,N-Diethylbenzamide is used as an insect repellent.

Synthesis Reference(s)

Chemistry Letters, 20, p. 615, 1991Journal of the American Chemical Society, 111, p. 8742, 1989 DOI: 10.1021/ja00205a039Tetrahedron Letters, 19, p. 5179, 1978 DOI: 10.1016/S0040-4039(01)85843-3

Safety Profile

Moderately toxic by ingestion andskin contact. When heated to decomposition it emits toxicfumes of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 1696-17-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,9 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1696-17:
(6*1)+(5*6)+(4*9)+(3*6)+(2*1)+(1*7)=99
99 % 10 = 9
So 1696-17-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO/c1-3-12(4-2)11(13)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3

1696-17-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L08427)  N,N-Diethylbenzamide, 99%   

  • 1696-17-9

  • 25g

  • 758.0CNY

  • Detail
  • Alfa Aesar

  • (L08427)  N,N-Diethylbenzamide, 99%   

  • 1696-17-9

  • 100g

  • 2310.0CNY

  • Detail
  • Alfa Aesar

  • (L08427)  N,N-Diethylbenzamide, 99%   

  • 1696-17-9

  • 25g

  • 758.0CNY

  • Detail
  • Alfa Aesar

  • (L08427)  N,N-Diethylbenzamide, 99%   

  • 1696-17-9

  • 100g

  • 2310.0CNY

  • Detail
  • Alfa Aesar

  • (L08427)  N,N-Diethylbenzamide, 99%   

  • 1696-17-9

  • 25g

  • 758.0CNY

  • Detail
  • Alfa Aesar

  • (L08427)  N,N-Diethylbenzamide, 99%   

  • 1696-17-9

  • 100g

  • 2310.0CNY

  • Detail
  • Alfa Aesar

  • (L08427)  N,N-Diethylbenzamide, 99%   

  • 1696-17-9

  • 25g

  • 758.0CNY

  • Detail
  • Alfa Aesar

  • (L08427)  N,N-Diethylbenzamide, 99%   

  • 1696-17-9

  • 100g

  • 2310.0CNY

  • Detail

1696-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name rebemide

1.2 Other means of identification

Product number -
Other names Rebemide

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:1696-17-9 SDS

1696-17-9Relevant articles and documents

Aminocarbonylation reaction using palladium complexes containing phosphorus-nitrogen ligands as catalysts

Aranda,Zolezzi,Valdebenito,Cáceres-Vásquez,Moya,Aguirre

, p. 2136 - 2137 (2013)

The catalytic activities of palladium complexes containing phosphorus-nitrogen ligands is reported. The catalysts studied showed high activities in the aminocarbonylation of aryl iodides. The palladium complexes reported activities between 100% and 58% in the aminocarbonylation reaction. The reactions are very selective for the double carbonylative amination of aryl halides. The major product is N,N-diethyl-?-oxo benzeneacetamide (96/4). The reaction was made under mild conditions of temperature and carbon monoxide pressure.

Heck reactions of ortho-substituted arenediazonium salts: Critical observations on electronic effects

Sengupta, Saumitra,Bhattacharyya, Sanchita

, p. 2035 - 2037 (2001)

An attempted Heck reaction of o-diethylamido phenyldiazonium tetrafluoroborate follows a unique radical-chain protodediazoniation pathway that is triggered by a facile 1,5-[H] shift of the derived aryl radical. Other ortho-substituted salts, irrespective of their redox potentials and structure, behave in the normal way.

Safer solvents for reactive organometallic reagents

Malinski, Thomas J.,Bergbreiter, David E.

, p. 3926 - 3929 (2018)

This paper describes the use of poly(α -olefin)s (PAOs) as safer alternatives to cyclohexane, hexanes, and heptane as solvents for alkyllithium reagents. While PAOs like any alkane are flammable, PAOs do not readily catch on fire because they contain 20 or more carbon atoms, a low volatility, and have a high flash point vis-à-vis alkanes like hexane. Also unlike conventional alkanes, PAOs can be quantitatively separated from polar organic solvents and polar organic products either by a simple gravity separation or by an extraction after a reaction. Any leaching of the PAO solvent into a polar phase during such a separation can be minimized by addition of small amounts of water to the polar phase. However, while these PAO solvents have some physical differences from conventional low molecular weight volatile alkanes, they otherwise behave like alkanes and alkyllithium reagents in these PAO solvents can used in their conventional reactions in these PAO solvents.

An experimentalist's guide to electrosynthesis: The Shono oxidation

Alfonso-Súarez, Paulino,Kolliopoulos, Athanasios V.,Smith, Jamie P.,Banks, Craig E.,Jones, Alan M.

, p. 6863 - 6867 (2015)

Electrosynthesis is a powerful method to functionalise organic molecules without the need to use chemical reagents or protecting groups, yet it is not widely used in synthesis. In this study, we investigated the Shono oxidation of a tertiary amide (electrochemical functionalisation of a C-H bond adjacent to an amide nitrogen atom), demonstrating the value of performing cyclic voltammetry, varying voltage and charge per mole, selection of electrolyte and electrode material. We demystify the process to demonstrate a simple relationship between oxidation potential, and charge transfer required, which affords a high conversion to the desired alpha-methoxylated product using an undivided experimental cell.

-

Brunet et al.

, p. 2199,2202 (1979)

-

-

Gilman

, p. 733 (1971)

-

One-pot synthesis of a highly disperse core-shell CuO-alginate nanocomposite and the investigation of its antibacterial and catalytic properties

Habibi, Hassan,Mansourinejhad, Sanam,Saberi, Dariush,Shadi, Ahmad

, p. 199 - 211 (2021/12/30)

In this study, sodium alginate was extracted from Sargassum algae, collected from coastal waters of Bushehr, Persian Gulf, Iran and used as a stabilizing and wrapping agent for CuO nanoparticles. The synthesized nanocomposite was characterized by some spectroscopic and microscopic techniques, such as IR, XRD, Uv-vis, BET, BJH, zeta potential, SEM, TEM, HR-TEM, and XPS. The antibacterial effects of the CuO-alginate nanocomposite against some bacteria, isolated from a burn wound, were evaluated. The results showed that this nanocomposite had better antibacterial effects than its components onPseudomonas aeruginosaATCC 27853,Staphylococcus aureusATCC 12600,Streptococcus pyogenesATCC 19615, andStaphylococcus epidermidisATCC 49461. Among these,Staphylococcus aureusATCC 12600 was the most sensitive one to this nanocomposite, with the lowest minimum inhibitory concentration (2.08 mg mL?1) observed. Moreover, the synthesized nanocomposite showed good catalytic activity in the oxidative coupling of carboxylic acids withN,N-dialkylformamides toward the synthesis of amides.

Iron-catalyzed oxidative amidation of acylhydrazines with amines

Wang, Yi-Jie,Zhang, Guo-Yu,Shoberu, Adedamola,Zou, Jian-Ping

, (2021/08/18)

A new approach for amide bond formation via a mild and efficient Iron-catalyzed cross-coupling reaction of acylhydrazines and amines using TBHP as oxidant is described. This protocol is compatible with a wide range of amines and acylhydrazines. In addition, the synthetic application of the reaction is presented.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1696-17-9