Welcome to LookChem.com Sign In|Join Free

CAS

  • or

5717-81-7

5717-81-7

Post Buying Request

5717-81-7 Suppliers

Recommended suppliersmore

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

5717-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5717-81-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,1 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5717-81:
(6*5)+(5*7)+(4*1)+(3*7)+(2*8)+(1*1)=107
107 % 10 = 7
So 5717-81-7 is a valid CAS Registry Number.
InChI:InChI=1/C24H21BrN4O3S/c1-2-3-10-31-19-7-4-15(5-8-19)22(30)29-24(33)27-18-6-9-21-20(12-18)28-23(32-21)16-11-17(25)14-26-13-16/h4-9,11-14H,2-3,10H2,1H3,(H2,27,29,30,33)

5717-81-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[[2-(5-bromopyridin-3-yl)-1,3-benzoxazol-5-yl]carbamothioyl]-4-butoxybenzamide

1.2 Other means of identification

Product number -
Other names androsteronehemisuccinate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5717-81-7 SDS

5717-81-7Downstream Products

5717-81-7Relevant articles and documents

Design of potent inhibitors for Schistosoma japonica glutathione S-transferase

Jao, Shu-Chuan,Chen, Jessica,Yang, Kelvin,Li, Wen-Shan

, p. 304 - 318 (2007/10/03)

We implemented both structure-based drug design and the concept of polyvalency to discover a series of potent and unsymmetrical Schistosoma japonicum glutathione S-transferase (SjGST) inhibitors 10-12. This strategy achieved not only an excellent enhancement (10- to 490-fold) in the inhibitory potency, compared to the monofunctional analogues 1-5, but was also an effective modification by selecting a hydrophobic moiety with a flexible linker. The designed compounds with a low micromolar hit demonstrate special values in refining the new generation of SjGST inhibitors. The stoichiometry of the binding is one inhibitor molecule per SjGST monomer via isothermal titration calorimetric measurement.

On the synthesis of 3-alpha-hydroxy-5-beta-androstanone-(17)-glucuronide in the rat liver

Staib,Albaum,Doenges

, p. 277 - 281 (2007/10/10)

-

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 5717-81-7