Welcome to LookChem.com Sign In|Join Free
  • or
The chemical compound "(1R)-3c-((R)-2-phenyl-butyryloxy)-1r-methyl-4t-isopropyl-cyclohexane" is a complex organic molecule with a cyclohexane ring as its central structure. It features a chiral center at the 1R position, indicating that the molecule has a specific three-dimensional arrangement of atoms. The compound includes a 3c-((R)-2-phenyl-butyryloxy) group, which is an ester derived from (R)-2-phenylbutyric acid, attached to the cyclohexane ring. Additionally, it has a methyl group at the 1r position and an isopropyl group at the 4t position, both of which contribute to the molecule's stereochemistry. (1R)-3c-((R)-2-phenyl-butyryloxy)-1r-methyl-4t-isopropyl-cyclohexane is characterized by its unique spatial arrangement and functional groups, which may have implications for its physical and chemical properties, as well as potential applications in various fields such as pharmaceuticals or materials science.

53483-40-2

Post Buying Request

53483-40-2 Suppliers

Recommended suppliers

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

53483-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53483-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,8 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53483-40:
(7*5)+(6*3)+(5*4)+(4*8)+(3*3)+(2*4)+(1*0)=122
122 % 10 = 2
So 53483-40-2 is a valid CAS Registry Number.

53483-40-2Downstream Products

53483-40-2Relevant academic research and scientific papers

Diethyl zinc catalyzed diastereoselective addition of ketenes to (S)-(+)-3-hydroxytetrahydrofuran

Tandon, Vishnu K.

, p. 5985 - 5987 (2007/10/03)

The reaction of (S)-(+)-3-hydroxytetrahydrofuran with phenyl methyl ketene in presence of n-BuLi and Et2Zn results in the formation of the diastereomeric esters (SS+SR) with a high degree of diastereoselectivity (98:2).

Kinetic Resolution of Racemic Carboxylic Acids and Alcohols with Homochiral Alcohols and Carboxylic Acids, Respectively, and the Mukaiyama or Palomo Reagents

Mazon, Angel,Najera, Carmen,Yus, Miguel,Heumann, Andreas

, p. 1455 - 1466 (2007/10/02)

The Mukaiyama and Palomo reagents have been used for the kinetic resolution of racemic carboxylic acids or alcohols with homochiral alcohols or carboxylic acids, respectively, in the presence of triethylamine.Thus, enantiomerically enriched carboxylic acids (e.e.68percent), alcohols (e.e.41percent) or diastereoisomerically enriched esters (d.e.84percent) are obtained.

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 53483-40-2