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38601-55-7

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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-(4-BROMOBENZYL)OXIME

    Cas No: 38601-55-7

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38601-55-7 Usage

Furan ring

A heterocyclic organic compound consisting of a benzene ring with one oxygen atom replaced by a furan ring (an oxygen atom double-bonded to two carbon atoms).

Multiple hydroxyl groups

The presence of multiple -OH groups, which are functional groups that can form hydrogen bonds and participate in various chemical reactions.

Methoxy group

A -OCH3 functional group, which is a methoxy group attached to an aromatic ring, providing additional steric hindrance and electronic effects.

Epoxide functional group

A three-membered cyclic ether with an oxygen atom in each ring, which is a reactive group due to its high strain and can participate in various chemical reactions.

Imine functional group

A nitrogen-carbon double bond (C=N) within a long aliphatic chain, which can undergo various reactions and contribute to the compound's biological activity.

Acetate group

A -COCH3 functional group, which is an ester derived from acetic acid, and can be hydrolyzed under certain conditions.

Bromobenzyl oxime moiety

A functional group containing a bromine atom attached to a benzyl group, which is connected to an oxime group (-C=N-OH). This moiety can be used for the synthesis of various pharmaceuticals and agrochemicals.

Hexahydroxy structure

The presence of six hydroxyl groups in the compound, which can contribute to its solubility, stability, and biological activity.

Heptamethyl structure

The presence of seven methyl groups attached to the compound, which can provide steric hindrance and influence the compound's lipophilicity.

Potential biological activities

Due to the complex structure and diverse functional groups, this compound may exhibit a wide range of biological activities, making it of interest for pharmaceutical or biochemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 38601-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,0 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38601-55:
(7*3)+(6*8)+(5*6)+(4*0)+(3*1)+(2*5)+(1*5)=117
117 % 10 = 7
So 38601-55-7 is a valid CAS Registry Number.
InChI:InChI=1/C45H53BrN2O13/c1-21-11-10-12-22(2)44(56)48-35-30(19-47-59-20-28-13-15-29(46)16-14-28)39(53)32-33(40(35)54)38(52)26(6)42-34(32)43(55)45(8,61-42)58-18-17-31(57-9)23(3)41(60-27(7)49)25(5)37(51)24(4)36(21)50/h10-19,21,23-25,31,36-37,41,47,50-52,54H,20H2,1-9H3,(H,48,56)/b11-10+,18-17+,22-12+,30-19+

38601-55-7SDS

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-[(4-bromo-benzyloxyimino)-methyl]-rifamycin

1.2 Other means of identification

Product number -
Other names 3-Formylrifamycin-SV-O-p-Brombenzyloxim

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:38601-55-7 SDS

38601-55-7Downstream Products

38601-55-7Relevant 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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