Welcome to LookChem.com Sign In|Join Free

CAS

  • or

627076-70-4

Post Buying Request

627076-70-4 Suppliers

Recommended suppliersmore

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

627076-70-4 Usage

General Description

(R)-2-hydroxy-2-phenylpropyl 4-methylbenzenesulfonate is a chemical compound consisting of a phenylpropyl group and a 4-methylbenzenesulfonate group. It is commonly used as an intermediate in the production of pharmaceuticals and other organic compounds. The compound has the potential to be used as a stabilizer and preservative in various products due to its ability to inhibit the growth of microorganisms. Additionally, it may have applications in the manufacturing of polymers and specialty chemicals. Overall, (R)-2-hydroxy-2-phenylpropyl 4-methylbenzenesulfonate has versatile properties and could be utilized in a variety of industries for different purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 627076-70-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,7,0,7 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 627076-70:
(8*6)+(7*2)+(6*7)+(5*0)+(4*7)+(3*6)+(2*7)+(1*0)=164
164 % 10 = 4
So 627076-70-4 is a valid CAS Registry Number.

627076-70-4Relevant articles and documents

Absolute Configuration of α-Methylstyrene Oxide: The Correct Absolute Configuration/Optical Rotation Corelation

Archelas,Furstoss

, p. 6112 - 6114 (1999)

-

Highly homogeneous stereocontrolled construction of quaternary hydroxyesters by addition of dimethylzinc to α-ketoesters promoted by chiral perhydrobenzoxazines and B(OEt)3

Infante, Rebeca,Nieto, Javier,Andres, Celia

supporting information; experimental part, p. 4375 - 4379 (2012/05/20)

A highly efficient enantioselective addition of Me2Zn to α-ketoesters, assisted by a chiral perhydro-1,3-benzoxazine ligand, is described. This novel catalytic system offers homogeneous elevated enantioselectivities in the preparation of α-hydroxyesters that bear a quaternary stereocenter, with a minor dependence on electronic and steric effects when aromatic, heteroaromatic, or aliphatic α-ketoesters are employed. The catalyst can be recovered and reused without loss of activity.

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 627076-70-4