Welcome to LookChem.com Sign In|Join Free
  • or
3-[[(Dodecyloxy)imino]methyl]rifamycin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38546-31-5

Post Buying Request

38546-31-5 Suppliers

Recommended suppliers

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

38546-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38546-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,5,4 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38546-31:
(7*3)+(6*8)+(5*5)+(4*4)+(3*6)+(2*3)+(1*1)=135
135 % 10 = 5
So 38546-31-5 is a valid CAS Registry Number.
InChI:InChI=1/C50H72N2O13/c1-11-12-13-14-15-16-17-18-19-20-25-63-51-27-35-40-45(58)38-37(44(35)57)39-47(33(7)43(38)56)65-50(9,48(39)59)62-26-24-36(61-10)30(4)46(64-34(8)53)32(6)42(55)31(5)41(54)28(2)22-21-23-29(3)49(60)52-40/h21-24,26-28,30-32,36,41-42,46,51,54-56,58H,11-20,25H2,1-10H3,(H,52,60)/b22-21+,26-24+,29-23+,35-27+

38546-31-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Formylrifamycin SV O-dodecyloxime

1.2 Other means of identification

Product number -
Other names rifaldehyde O-dodecyl-oxime

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:38546-31-5 SDS

38546-31-5Downstream Products

38546-31-5Relevant academic research and scientific papers

Oximes of 3 formylrifamycin SV. Synthesis, antibacterial activity, and other biological properties

Cricchio,Lancini,Tamborini,Sensi

, p. 396 - 403 (2007/10/06)

The synthesis of the oximes of 3 formylrifamycin SV and the preparation of some of the O substituted hydroxylamine intermediates are described. The chemical and physical characteristics, the antibacterial activity on wild type and rifampicin resistant strains, and other biological properties of the new derivatives are reported. Structure activity relationships show that increasing the lipophilicity of the oxime substituent decreases the antibacterial activity, both in vitro and in experimental infection, whereas inhibition of a rifampicin resistant strain of S. aureus and of several transcribing enzymes is increased.

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 38546-31-5