Welcome to LookChem.com Sign In|Join Free
  • or
(2S,16S,17S,18R,19R,20R,21S,22R,23S,24E)-8-[(2-aminoethyl)sulfanyl]-5,6,9,17,19-pentahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13724-90-8

Post Buying Request

13724-90-8 Suppliers

Recommended suppliers

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

13724-90-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13724-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,2 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13724-90:
(7*1)+(6*3)+(5*7)+(4*2)+(3*4)+(2*9)+(1*0)=98
98 % 10 = 8
So 13724-90-8 is a valid CAS Registry Number.

13724-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Rifamycin, 3-((2-aminoethyl)thio)-

1.2 Other means of identification

Product number -
Other names 3-(2-aminoethylthio)rifamycin SV

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:13724-90-8 SDS

13724-90-8Relevant academic research and scientific papers

Synthesis and Activity Studies on 3-(Carboxyalkylthio)rifamycin S Derivatives

Cellai, Luciano,Martuccio, Concetta,Marzano, Marina,Onori, Alberto Mochi,Mannina, Luisa,et al.

, p. 317 - 324 (2007/10/03)

A series of rifamycin S derivatives carrying at C(3) an aliphatic side-chain of variable length terminating with a carboxyl has been synthesised; in particular, five of these compounds carry a terminal dipeptide.The aim was to prepare potential bifunctional HIV-1 reverse transcriptase inhibitors, able both to bind at the non-nucleoside inhibitors binding site, through the chromophore rings, and to interfere with the catalytic centre, through the side-chain terminal carboxyl.Some of the compounds display an interesting inhibitory power (IC50 45-60 μM).In addition, a few of these derivatives have been also tested as potential antibacterial agents, and showed a good level of activity toward Gram-positive bacteria.

Thiazo rifamycins-I. Structure and synthesis of rifamycins p, q and verde, novel metabolites from mutants of nocardia mediterranea

Cricchio,Antonini,Lancini,Tamborini,White,Martinelli

, p. 1415 - 1421 (2007/10/02)

Structures 1, 2 and 3 have been assigned to rifamycins P, Q and Verde, novel metabolites isolated from a mutant strain of Nocardia mediterranea both on the basis of spectroscopic evidence (UV, IR, MS, 1H and 13C NMR) in comparison with the model compounds rifamycin S (4), rifampicin (5) and 4-dimethylamino-4-deoxy-rifamycin SV (6), and of an unambiguous synthesis from rifamycin S (4).

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 13724-90-8