Welcome to LookChem.com Sign In|Join Free

CAS

  • or

91410-69-4

Post Buying Request

91410-69-4 Suppliers

Recommended suppliersmore

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

91410-69-4 Usage

Description

(R)-1-(adamantyl)ethanol, with the molecular formula C12H20O, is a colorless liquid characterized by a mild odor. It is a chemical compound that features a unique molecular structure due to the presence of an adamantyl group, which provides steric hindrance. This characteristic makes it a valuable chiral building block in organic synthesis. Known for its high boiling point and good solubility in organic solvents, (R)-1-(adamantyl)ethanol is a versatile and useful compound in a range of chemical processes. It also holds potential pharmaceutical applications due to its intriguing structural features and biological properties.

Uses

Used in Pharmaceutical Industry:
(R)-1-(adamantyl)ethanol is used as a chiral building block for the synthesis of various pharmaceutical compounds. Its unique molecular structure and steric hindrance contribute to the development of new drugs with improved efficacy and selectivity.
Used in Pesticide Industry:
In the pesticide industry, (R)-1-(adamantyl)ethanol is utilized as an intermediate in the synthesis of bioactive molecules. Its properties allow for the creation of pesticides with enhanced target specificity and reduced environmental impact.
Used in Organic Synthesis:
(R)-1-(adamantyl)ethanol is used as a versatile compound in organic synthesis, taking advantage of its high boiling point and good solubility in organic solvents. This enables its application in a wide range of chemical reactions and processes.
Used in Industrial Product Manufacturing:
(R)-1-(adamantyl)ethanol is employed in the production of various industrial products, leveraging its unique structural features and properties to enhance the performance and characteristics of the final products.

Check Digit Verification of cas no

The CAS Registry Mumber 91410-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,1 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91410-69:
(7*9)+(6*1)+(5*4)+(4*1)+(3*0)+(2*6)+(1*9)=114
114 % 10 = 4
So 91410-69-4 is a valid CAS Registry Number.

91410-69-4Relevant articles and documents

Kinetic Resolution of Neopentylic Secondary Alcohols by Cu-H-Catalyzed Enantioselective Silylation with Hydrosilanes

Oestreich, Martin,Papadopulu, Zaneta

supporting information, p. 438 - 441 (2021/01/13)

A nonenzymatic kinetic resolution of sterically congested alcohols having a quaternary carbon atom in the β-position is reported. The catalyst system CuCl/NaOtBu/(R,R)-Ph-BPE together with a 3,5-xylyl-substituted tertiary hydrosilane enable enantioselective silylation of the hydroxy group. Several alcohols are obtained with good to excellent selectivity factors, and there are no other known straightforward methods to access these motifs.

PROCESS FOR THE PREPARATION OF ORGANIC COMPOUNDS WITH IMIDE CATALYSTS

-

, (2008/06/13)

(A) A compound capable of forming a stable radical and selected from (A1) oxygen-atom-containing compounds each having a carbon-hydrogen bond at the adjacent position to an oxygen atom, (A2) carbonyl-group-containing compounds, and (A3) compounds each having a hydrocarbon group with a methine carbon atom is allowed to react with (B) a radical scavenging compound selected from, for example, (B1) unsaturated compounds, and (B2) compounds each having a hydrocarbon group with a methine carbon atom, in the presence of molecular oxygen by catalysis of, for example, an imide compound shown by the following formula (1): wherein each of R1 and R2 is a hydrogen atom or the like, where R1 and R2 may be combined to form a double bond, or an aromatic or non-aromatic ring; X is an oxygen atom or a hydroxyl group, to yield a product of an addition or substitution reaction of the compound (A) and the compound (B) or its oxidized product. The process can efficiently produce a variety of organic compounds by an addition or substitution reaction using molecular oxygen under mild conditions.

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 91410-69-4