Welcome to LookChem.com Sign In|Join Free

CAS

  • or

699-08-1

Post Buying Request

699-08-1 Suppliers

Recommended suppliersmore

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

699-08-1 Usage

Chemical Properties

Off-white low melting solid

Uses

Different sources of media describe the Uses of 699-08-1 differently. You can refer to the following data:
1. 4-Iodophenetole may be used as one of the components in the synthesis of bis(4-ethoxyphenyl)amine.
2. Intermediates of Liquid Crystals
3. suzuki reaction

Check Digit Verification of cas no

The CAS Registry Mumber 699-08-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 699-08:
(5*6)+(4*9)+(3*9)+(2*0)+(1*8)=101
101 % 10 = 1
So 699-08-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H9IO/c1-2-10-8-5-3-7(9)4-6-8/h3-6H,2H2,1H3

699-08-1 Well-known Company Product Price

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

  • (B21644)  4-Iodophenetole, 97%   

  • 699-08-1

  • 5g

  • 293.0CNY

  • Detail
  • Alfa Aesar

  • (B21644)  4-Iodophenetole, 97%   

  • 699-08-1

  • 25g

  • 971.0CNY

  • Detail
  • Alfa Aesar

  • (B21644)  4-Iodophenetole, 97%   

  • 699-08-1

  • 100g

  • 2615.0CNY

  • Detail

699-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Iodophenetole

1.2 Other means of identification

Product number -
Other names Benzene, 1-ethoxy-4-iodo-

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:699-08-1 SDS

699-08-1Relevant articles and documents

Synthesis, Crystal Structure, and Photophysical Properties of Nickel Complex from Triphenylamine Schiff Base Ligand

Chen, Jiang,Wang, Hui,Jin, Zhepeng,Gao, Bingfei,Wu, Jieying,Tian, Yupeng

, p. 896 - 901 (2016)

A novel Schiff base ligand L and its mononuclear nickel complex Ni(L)2(SCN)2 were designed, synthesized and characterized by elemental analysis, IR spectra, MS, 1H-NMR spectroscopy, and single-crystal X-ray diffraction analysis. The crystals of L and Ni(L)2(SCN)2 belong to orthorhombic crystal system with the space group of P212121 for L and Pbcn for Ni(L)2(SCN)2, respectively. The center atom Ni(II) is coordinated with six nitrogen atoms in a distorted octahedron coordination environment. The four N atoms of them are from the two independent ligands and the other two nitrogen atoms from two SCN-. Their photophysical properties of the ligand and its Ni(II) complex were investigated and interpreted on the basis of theoretical calculations (TD-DFT).

Organic hole transport material and preparation method and application thereof

-

Paragraph 0033-0035, (2019/07/01)

The invention provides an organic hole transport material and a preparation method and application thereof. The structural general formula of the organic hole transport material is shown in the specification, and in the formula, R is ethyl, propyl, isopropyl or butyl. The preparation method is simple and easy to implement, the structure is definite, and the prepared organic hole transport materialhas high photoelectric conversion efficiency and can be applied to perovskite solar cells.

Photocatalytic Oxidative Iodination of Electron-Rich Arenes

Narobe, Rok,Düsel, Simon J. S.,Iskra, Jernej,K?nig, Burkhard

supporting information, p. 3998 - 4004 (2019/07/17)

A visible-light-mediated oxidative iodination of electron-rich arenes has been developed. 2.5 mol% of unsubstituted anthraquinone as photocatalyst were used in combination with elementary iodine, trifluoroacetic acid and oxygen as the terminal oxidant. The iodination proceeds upon irradiation in non- or weakly-electron donating solvents (DCM, DCE and benzene) wherein a spectral window in strongly coloured iodine solutions can be observed at around 400 nm. The method provides good to excellent yields (up to 98%) and shows excellent regioselectivity and good functional group tolerance (triple bonds, ketone, ester, amide). Moreover, the photo-iodination was also upscaled to a 5 mmol scale (1.1 g). Mechanistic investigations by intermediate trapping and competition experiments indicate a photocatalytic arene oxidation and the subsequent reaction with iodine as a likely mechanistic pathway. (Figure 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 699-08-1