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72393-97-6

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72393-97-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72393-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,9 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 72393-97:
(7*7)+(6*2)+(5*3)+(4*9)+(3*3)+(2*9)+(1*7)=146
146 % 10 = 6
So 72393-97-6 is a valid CAS Registry Number.

72393-97-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxycarbonylrifamycin S

1.2 Other means of identification

Product number -
Other names 3-(carbomethoxy)rifamycin S

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:72393-97-6 SDS

72393-97-6Downstream Products

72393-97-6Relevant articles and documents

A Study on the Structures of 3-Methoxycarbonylrifamycins by X-Ray Crystallography and 1H Nuclear Magnetic Resonance Spectroscopy

Cellai, Luciano,Cerrini, Silvio,Segre, Annalaura,Brufani, Mario,Fedeli, Walter,Vaciago, Alessandro

, p. 1633 - 1640 (2007/10/02)

The structures of 3-methoxycarbonylrifamycins were studied by X-ray crystallography and 1H n.m.r. spectroscopy.The resulrs obtained by the two different methods are consistent.The comparison with the conformations of some ansamycins in the solid state shows that in this and in other active compounds the central part of the ansa-chain, directly involved in the inhibitory interaction with the bacterial enzyme DNA-dependent RNA polymerase, remains in general the same, while large conformational changes may occur at the junctions of the ansa-chain with the chromophore-rings, thus generating four kinds of conformers.Therefore the 3-methoxycarbonyl substituent does not seem to exert any influence on the conformation of the ansa-chain which can be related to the decrease of the antibacterial activity of 3-methoxycarbonylrifamycin S.

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