Welcome to LookChem.com Sign In|Join Free

CAS

  • or
[3,4-bis(tert-butyl-dimethyl-silanyloxy)-phenyl]methanol is a chemical compound that belongs to the class of organosilicon compounds. It is a derivative of phenol and has two tert-butyl-dimethyl-silanyloxy groups attached to the 3 and 4 positions of the phenyl ring. [3,4-bis(tert-butyl-dimethyl-silanyloxy)-phenyl]methanol also contains a methanol group attached to the phenyl ring. This unique structure and properties make it a promising candidate for various applications in materials science and pharmaceutical research.

1036243-79-4

Post Buying Request

1036243-79-4 Suppliers

Recommended suppliersmore

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

1036243-79-4 Usage

Uses

Used in Chemical Synthesis:
[3,4-bis(tert-butyl-dimethyl-silanyloxy)-phenyl]methanol is used as a building block for the synthesis of other organosilicon compounds. Its unique structure allows for the creation of a wide range of compounds with potential applications in various industries.
Used in Organic Synthesis:
[3,4-bis(tert-butyl-dimethyl-silanyloxy)-phenyl]methanol is used as a reagent in organic synthesis. Its properties make it a valuable component in the development of new organic compounds, which can be utilized in various fields, including pharmaceuticals and materials science.
Used in Materials Science:
[3,4-bis(tert-butyl-dimethyl-silanyloxy)-phenyl]methanol is used as a component in the development of new materials. Its unique structure and properties can contribute to the creation of advanced materials with improved characteristics, such as enhanced stability, durability, or specific functional properties.
Used in Pharmaceutical Research:
[3,4-bis(tert-butyl-dimethyl-silanyloxy)-phenyl]methanol is used in pharmaceutical research for the development of new drugs and drug delivery systems. Its unique structure and properties can be harnessed to create novel therapeutic agents or improve the efficacy and safety of existing medications.
Used in Research and Development:
[3,4-bis(tert-butyl-dimethyl-silanyloxy)-phenyl]methanol is used in research and development for the exploration of its potential applications and properties. This can lead to the discovery of new uses and advancements in various industries, including materials science, pharmaceuticals, and chemical synthesis.
It is important to handle and store [3,4-bis(tert-butyl-dimethyl-silanyloxy)-phenyl]methanol in accordance with proper safety guidelines to prevent any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 1036243-79-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,2,4 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1036243-79:
(9*1)+(8*0)+(7*3)+(6*6)+(5*2)+(4*4)+(3*3)+(2*7)+(1*9)=124
124 % 10 = 4
So 1036243-79-4 is a valid CAS Registry Number.

1036243-79-4Relevant articles and documents

Highly sulphated cellulose: a versatile, reusable and selective desilylating agent for deprotection of alcoholic TBDMS ethers

Dachavaram, Soma Shekar,Penthala, Narsimha R.,Calahan, Julie L.,Munson, Eric J.,Crooks, Peter A.

, p. 6057 - 6062 (2018/09/06)

A mild, efficient and rapid protocol was developed for the deprotection of alcoholic TBDMS ethers using a recyclable, eco-friendly highly sulphated cellulose sulphate acid catalyst in methanol. This acid catalyst selectively cleaves alcoholic TBDMS ethers in bis-TBDMS ethers containing both alcoholic and phenolic TBDMS ether moieties.

Resveratrol derivative containing fluorine group, and preparation method and application

-

, (2017/09/01)

The invention belongs to the technical field of medicines and discloses a resveratrol derivative containing a fluorine group, and a preparation method and an application. The resveratrol derivative has the structural characteristics as shown in a general

Total synthesis of artochamins F, H, I, and J through cascade reactions

Nicolaou,Lister, Troy,Denton, Ross M.,Gelin, Christine F.

, p. 4736 - 4757 (2008/09/21)

A concise and efficient cascade-based total synthesis of artochamins F, H, I, and J is described. The potential biogenetic connection between artochamin F, or a derivative thereof, and artochamins H, I, and J, through an unusual formal [2+2] cycloaddition

Cascade reactions involving formal [2+2] thermal cycloadditions: Total synthesis of artochamins F, H, I, and J

Nicolaou,Lister, Troy,Denton, Ross M.,Gelin, Christine F.

, p. 7501 - 7505 (2008/09/17)

(Chemical Equation Presented) State of the artochamins: Total syntheses of artochamins F (1), H (2), I (3), and J (4; see scheme) have been achieved through a flexible and expedient strategy that features a cascade sequence involving two concurrent [3,3]

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 1036243-79-4