Welcome to LookChem.com Sign In|Join Free
  • or
2-Acetyl-5-benzyloxy-pentanoic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99701-67-4

Post Buying Request

99701-67-4 Suppliers

Recommended suppliers

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

99701-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99701-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,7,0 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99701-67:
(7*9)+(6*9)+(5*7)+(4*0)+(3*1)+(2*6)+(1*7)=174
174 % 10 = 4
So 99701-67-4 is a valid CAS Registry Number.

99701-67-4Relevant academic research and scientific papers

Asymmetric Aza-Wacker-Type Cyclization of N-Ts Hydrazine-Tethered Tetrasubstituted Olefins: Synthesis of Pyrazolines Bearing One Quaternary or Two Vicinal Stereocenters

Kou, Xuezhen,Shao, Qihang,Ye, Chenghao,Yang, Guoqiang,Zhang, Wanbin

supporting information, p. 7587 - 7597 (2018/06/04)

We have developed an asymmetric aza-Wacker-type cyclization of N-Ts hydrazine-tethered tetrasubstituted olefins, affording optically active pyrazolines bearing chiral tetrasubstituted carbon stereocenters. This reaction is tolerant to a broad range of substrates under mild reaction conditions, giving the desired chiral products with high enantioselectivities. Generation of two vicinal stereocenters on the C=C double bonds was also achieved with high selectivities, a process which has been rarely studied for Wacker-type reactions. A mechanistic study revealed that this aza-Wacker-type cyclization undergoes a syn-aminopalladation process. It was also found that for substrates bearing two linear alkyl substituents on the outer carbon atom of the olefin, both of which are larger than a methyl group, the alkyl substituent that is cis to the intranucleophilic group participates more readily in β-hydride elimination. When one of the two alkyl substituents on the outer carbon atom of the olefin is a methyl group, β-hydride elimination proceeds selectively at the methylene side, thus both diastereomers can be prepared via switching the configuration of the olefin. Furthermore, the product can be converted to a pharmaceutical compound in high yields over three steps.

Formation of bridge-methylated decalins by antibody-catalyzed tandem cationic cyclization

Hasserodt, Jens,Janda, Kim D.,Lerner, Richard A.

, p. 5993 - 5998 (2007/10/03)

We report the antibody catalysis of an electrophilic tandem ring forming process that yields a bicyclic ring system at neutral pH. Three closely related decalin systems that represent rings A and B of the steroid nucleus account for 50% of the overall pro

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 99701-67-4