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13292-54-1

13292-54-1

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  • 2,7-(Epoxypentadeca(1,11,13)trienimino)naphtho(2,1-b)furan-1,11(2H)-dione, 3-formyl-5,6,9,17,19,21-hexahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-, 21-acetate, O-methyloxime cas 13292-54-1

    Cas No: 13292-54-1

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13292-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13292-54-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,9 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13292-54:
(7*1)+(6*3)+(5*2)+(4*9)+(3*2)+(2*5)+(1*4)=91
91 % 10 = 1
So 13292-54-1 is a valid CAS Registry Number.
InChI:InChI=1/C39H50N2O13/c1-17-12-11-13-18(2)38(49)41-29-24(16-40-51-10)33(46)26-27(34(29)47)32(45)22(6)36-28(26)37(48)39(8,54-36)52-15-14-25(50-9)19(3)35(53-23(7)42)21(5)31(44)20(4)30(17)43/h11-17,19-21,25,30-31,35,40,43-45,47H,1-10H3,(H,41,49)/b12-11+,15-14+,18-13u,24-16-

13292-54-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-(Epoxypentadeca(1,11,13)trienimino)naphtho(2,1-b)furan-1,11(2H)-dione, 3-formyl-5,6,9,17,19,21-hexahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-, 21-acetate, O-methyloxime

1.2 Other means of identification

Product number -
Other names 3-Formylrifamycin SV O-methyloxim

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:13292-54-1 SDS

13292-54-1Downstream Products

13292-54-1Relevant articles and documents

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.

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