Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Cyclopentanecarboxylic acid, 2-[[(1R)-1-phenylethyl]amino]-, methyl ester, (1S,2R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

683774-10-9

Post Buying Request

683774-10-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • Cyclopentanecarboxylic acid, 2-[[(1R)-1-phenylethyl]amino]-, methyl ester, (1S,2R)-

    Cas No: 683774-10-9

  • Need to discuss

  • No requirement

  • Adequate

  • Joyochem Co., Ltd.
  • Contact Supplier
  • Cyclopentanecarboxylic acid, 2-[[(1R)-1-phenylethyl]amino]-, methyl ester, (1S,2R)-

    Cas No: 683774-10-9

  • Need to discuss

  • No requirement

  • Adequate

  • Chemlyte Solutions
  • Contact Supplier

683774-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 683774-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,3,7,7 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 683774-10:
(8*6)+(7*8)+(6*3)+(5*7)+(4*7)+(3*4)+(2*1)+(1*0)=199
199 % 10 = 9
So 683774-10-9 is a valid CAS Registry Number.

683774-10-9Downstream Products

683774-10-9Relevant articles and documents

Synthesis, preliminary biological evaluation and molecular modeling of some new heterocyclic inhibitors of TACE

Sengupta, Prabal,Puri, Chetan S.,Chokshi, Hemant A.,Sheth, Chetana K.,Midha, Ajay S.,Chitturi, Trinadha Rao,Thennati, Rajamannar,Murumkar, Prashant R.,Yadav, Mange Ram

, p. 5549 - 5555 (2011)

Central heteroaryl ring analogues belonging to a series of potent hydroxamate TACE inhibitors were synthesized. The TACE inhibitory activities of these compounds were evaluated by in vitro WBA and in silico molecular modeling studies using crystal structure of human TACE. Compound 14 showed very good in vitro inhibition, supported by the in silico docking studies.

Asymmetric catalytic hydrogenation process for preparation of chiral cyclic beta-aminoesters

-

Page 11, (2008/06/13)

A novel process for the asymmetric synthesis of substituted cyclic β-amino-carboxylates of the type shown in the specification from appropriate β-enamino-ester starting materials is described. These compounds are useful as intermediates for MMP and TACE i

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 683774-10-9