Welcome to LookChem.com Sign In|Join Free
  • or
{(S)-2-[4-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-1-hydroxymethyl-ethyl}-carbamic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

179680-94-5

Post Buying Request

179680-94-5 Suppliers

Recommended suppliers

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

179680-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 179680-94-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,6,8 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 179680-94:
(8*1)+(7*7)+(6*9)+(5*6)+(4*8)+(3*0)+(2*9)+(1*4)=195
195 % 10 = 5
So 179680-94-5 is a valid CAS Registry Number.

179680-94-5Relevant academic research and scientific papers

Synthesis of MeO-PEG2000-supported chiral ferrocenyl oxazoline carbinol ligand and its application in asymmetric catalysis

Zhao, Wen-Xian,Liu, Guan-Jun,Wang, Jingjing,Li, Feng,Liu, Lantao

, p. 1133 - 1144 (2016)

A simple method for the synthesis of a MeO-PEG-supported chiral ferrocenyl oxazoline carbinol ligand has been developed. The chiral ligand was successfully applied to the catalytic asymmetric addition of diethylzinc to aryl aldehydes, affording secondary alcohols in high yields and with excellent enantioselectivities (up to 94% ee). The chiral ligand can be recovered and reused twice with no apparent loss of catalyst efficiency.

The total synthesis of the diepoxycyclohexanone antibiotic aranorosin and novel synthetic analogues

McKillop, Alexander,McLaren, Lee,Taylor, Richard J. K.,Watson, Robert J.,Lewis, Norman J.

, p. 1385 - 1393 (2007/10/03)

A short synthesis of the novel antibiotic aranorosin in chiral form is described which employs (i) a novel hypervalent iodine-mediated oxidative hydroxylation of a tyrosinal derivative and (ii) a stereocontrolled cis-bisepoxidation in the key steps. A similar procedure was employed to prepare 6′-epiaranorosin, and hence establish the stereochemistry of the natural compound, and to prepare novel aranorosin analogues. An organometallic route is described which gives desamidoaranorosin.

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 179680-94-5