Welcome to LookChem.com Sign In|Join Free
  • or
sorangicin A is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100415-25-6

Post Buying Request

100415-25-6 Suppliers

Recommended suppliers

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

100415-25-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100415-25-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,1 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100415-25:
(8*1)+(7*0)+(6*0)+(5*4)+(4*1)+(3*5)+(2*2)+(1*5)=56
56 % 10 = 6
So 100415-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C47H66O11/c1-30(17-14-15-23-44(50)51)27-31(2)47-40-26-25-34(54-47)18-10-6-5-7-11-19-35(48)46(53)43-28-36(49)32(3)37(56-43)21-16-22-38-33(4)41-29-42(55-38)39(57-41)20-12-8-9-13-24-45(52)58-40/h6,8-13,16,19-20,22,24-27,30,32-43,46-49,53H,5,7,14-15,17-18,21,23,28-29H2,1-4H3,(H,50,51)/b9-8-,10-6-,19-11-,20-12-,22-16-,24-13-,31-27-

100415-25-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-sorangicin A

1.2 Other means of identification

Product number -
Other names Sesbanimide

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:100415-25-6 SDS

100415-25-6Related news

A short convergent synthesis of the [3.2.1]dioxabicyclooctane subunit of sorangicin A (cas 100415-25-6) via regioselective epoxide opening07/28/2019

In this paper, we disclose the synthesis of the dioxabicyclo[3.2.1]octane subunit of the potent antibiotic sorangicin A. The synthesis was achieved in a convergent manner in 8 steps. Regio- and stereoselective intermolecular epoxide opening, ring-closing metathesis and iodo-etherification are ke...detailed

100415-25-6Relevant academic research and scientific papers

Total synthesis of (+)-sorangicin A

Smith III, Amos B.,Dong, Shuzhi,Brenneman, Jehrod B.,Fox, Richard J.

supporting information; experimental part, p. 12109 - 12111 (2010/01/30)

(Chemical Equation Presented) The final synthetic challenges associated with (+)-sorangicin A have been overcome, thus leading to the first total synthesis of this complex macrolide antibiotic. Highlights of the highly convergent synthesis include two Jul

Antibiotics from Gliding Bacteria, XLII. Chemical Modification of Sorangicin A and Structure - Activity Relationship I: Carboxyl and Hydroxyl Group Derivatives

Jansen, Rolf,Schummer, Dietmar,Irschik, Herbert,Hoefle, Gerhard

, p. 975 - 988 (2007/10/02)

The synthesis of selectively protected sorangicin A derivatives and their application in the modification of the hydroxyl groups and the carboxyl group in sorangicin A (1) is described.Esters, amides, and sorangicins modified at the hydroxyl groups were prepared and their activities against Staphylococcus aureus, Escherichia coli, and their in vitro inhibition of RNA polymerase were examined.Although no sorangicin A derivatives with superior biological activity were observed, some derivatives completely retained their antibiotic activity or were slightly improved in their activity with certain strains.

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 100415-25-6