Welcome to LookChem.com Sign In|Join Free

CAS

  • or

127561-33-5

Post Buying Request

127561-33-5 Suppliers

Recommended suppliersmore

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

127561-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127561-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,6 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 127561-33:
(8*1)+(7*2)+(6*7)+(5*5)+(4*6)+(3*1)+(2*3)+(1*3)=125
125 % 10 = 5
So 127561-33-5 is a valid CAS Registry Number.

127561-33-5Relevant articles and documents

Supported iron catalysts for Michael addition reactions

Ye, Rong,Faucher, Franco F.,Somorjai, Gabor A.

, p. 65 - 71 (2018/02/13)

Heterogeneous catalysts have been widely used for chemical transformations and offer easy product separation in addition to their high activity. Iron is an earth-abundant metal, but it has not been studied thoroughly as heterogeneous catalysts for organic

The discovery of novel cyclohexylamide CCR2 antagonists

Lanter, James C.,Markotan, Thomas P.,Zhang, Xuqing,Subasinghe, Nalin,Kang, Fu-An,Hou, Cuifen,Singer, Monica,Opas, Evan,McKenney, Sandra,Crysler, Carl,Johnson, Dana,Molloy, Christopher J.,Sui, Zhihua

scheme or table, p. 7496 - 7501 (2012/02/13)

As a result of further SAR studies on a piperidinyl piperidine scaffold, we report the discovery of compound 44, a potent, orally bioavailable CCR2 antagonist. While having some in vitro hERG activity, this molecule was clean in an in vivo model of QT pro

α1b-adrenergic receptor antagonists

-

Page/Page column 78, (2010/11/30)

There are provided compounds represented by the general formula (I): [wherein Ar is indole etc., R1is hydrogen etc., B is bond, or B—N—R1forms a ring structure and is piperidine etc., n is 0, 1, etc., A is trimethylene, butylene, etc., Q is piperidine, isoindoline, etc.], or pharmacologically acceptable acid addition salts thereof, and α1B adrenoceptor antagonists composed of these substances. The invented compounds are antagonists having high affinity for α1B adrenoceptor and are useful as pharmaceutical agents for use in prophylaxis/therapy of diseases (e.g., hypertension) in which α1B adrenoceptor is involved or as pharmacological tools for elucidation of physiological activities mediated by α1B adrenoceptor.

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 127561-33-5