Welcome to LookChem.com Sign In|Join Free
  • or
2-(4-chlorophenyl)-9,9-dimethyl-9H-fluorene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1221237-82-6

Post Buying Request

1221237-82-6 Suppliers

Recommended suppliers

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

1221237-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1221237-82-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,2,3 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1221237-82:
(9*1)+(8*2)+(7*2)+(6*1)+(5*2)+(4*3)+(3*7)+(2*8)+(1*2)=106
106 % 10 = 6
So 1221237-82-6 is a valid CAS Registry Number.

1221237-82-6Relevant academic research and scientific papers

Organic Light Emitting Material and Organic Light Emitting Diode Having The Same

-

Paragraph 0338-0341, (2021/11/02)

The present invention relates to a compound derivative for an organic electroluminescent device and an organic electroluminescent device using the same. The present invention relates to an aromatic compound including an indolocarbazolyl group and a spirob

Organic Light Emitting Material and Organic Light Emitting Diode Having The Same

-

Paragraph 0184-0187, (2021/11/02)

The present invention relates to a compound derivative for an organic electroluminescent device and an organic electroluminescent device using the same. The present invention relates to an aromatic compound including an indolocarbazolyl group and a spirobifluorenyl group, and more particularly, to an aromatic compound including an indolocarbazolyl group and a spirobifluorenyl group.

Heterocyclic compound and organic electroluminescent device thereof

-

Paragraph 0144-0147, (2021/11/21)

The invention provides a heterocyclic compound and an organic electroluminescent device thereof. Belong to organic electroluminescence technical field. The heterocyclic compound provided by the invention has relatively high electron mobility and good hole

2-subtituted fluorene-based compound, hole transport material including the same, and organic electronic device including the same in a hole transport layer

-

Paragraph 0234-0239, (2020/06/30)

The present invention addresses the problems of providing a compound that can be used as a hole transport material having excellent hole injection or transport performance, electron blocking performance, light stability, electrical stability, and thermal stability, providing a hole transport material containing the compound, and an organic electronic device including an organic EL element or an organic photoelectric conversion element provided with a hole transport layer containing the compound, particularly an organic electronic device including an organic EL element having a long lifetime and high luminous efficiency. A compound is represented by general formula (1-1); in the formula, R1 to R6 and Ara to Arc are as defined in the specification.

HETERO-CYCLIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

-

Paragraph 0224-0226, (2016/10/08)

The present invention provides a heterocyclic compound, and an organic light emitting device comprising the same. The heterocyclic compound is represented by chemical formula 1. The compound can improve efficiency and/or lifespan properties in the organic

Gold-catalyzed oxidative coupling of arylsilanes and arenes: Origin of selectivity and improved precatalyst

Ball, Liam T.,Lloyd-Jones, Guy C.,Russell, Christopher A.

supporting information, p. 254 - 264 (2014/01/23)

The mechanism of gold-catalyzed coupling of arenes with aryltrimethylsilanes has been investigated, employing an improved precatalyst (thtAuBr3) to facilitate kinetic analysis. In combination with linear free-energy relationships, kinetic isotope effects, and stoichiometric experiments, the data support a mechanism involving an Au(I)/Au(III) redox cycle in which sequential electrophilic aromatic substitution of the arylsilane and the arene by Au(III) precedes product-forming reductive elimination and subsequent cycle-closing reoxidation of the metal. Despite the fundamental mechanistic similarities between the two auration events, high selectivity is observed for heterocoupling (C-Si then C-H auration) over homocoupling of either the arylsilane or the arene (C-Si then C-Si, or C-H then C-H auration); this chemoselectivity originates from differences in the product-determining elementary steps of each electrophilic substitution. The turnover-limiting step of the reaction involves associative substitution en route to an arene π-complex. The ramifications of this insight for implementation of the methodology are discussed.

NOVEL COMPOUND AND ORGANIC ELECTRONIC DEVICE USING SAME

-

Page/Page column 33, (2011/08/03)

The present invention relates to a novel compound and an organic light emitting device using the compound, and the compound according to the present invention may largely improve a life span, efficiency, electrochemical stability and thermal stability of the organic light emitting device.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1221237-82-6