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N',N'-Di(desmethyl) Azithromycin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

612069-27-9

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  • (2R,3S,4R,5R,8R,10S,11R,12S,13S,14R)-11-[(4-amino-3-hydroxy-6-methyloxan-2-yl)oxy]-2-ethyl-3,4,10-trihydroxy-13-[(5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl)oxy]-3,5,6,8,10,12,14-heptamethyl-1-oxa-6-az

    Cas No: 612069-27-9

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612069-27-9 Usage

Uses

Different sources of media describe the Uses of 612069-27-9 differently. You can refer to the following data:
1. A metabolite of Azithromycin.
2. A metabolite of Azithromycin. Azithromycin Impurity E

Check Digit Verification of cas no

The CAS Registry Mumber 612069-27-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,2,0,6 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 612069-27:
(8*6)+(7*1)+(6*2)+(5*0)+(4*6)+(3*9)+(2*2)+(1*7)=129
129 % 10 = 9
So 612069-27-9 is a valid CAS Registry Number.
InChI:InChI=1/C36H68N2O12/c1-13-25-36(10,44)29(40)22(6)38(11)17-18(2)15-34(8,43)31(50-33-27(39)24(37)14-19(3)46-33)20(4)28(21(5)32(42)48-25)49-26-16-35(9,45-12)30(41)23(7)47-26/h18-31,33,39-41,43-44H,13-17,37H2,1-12H3/t18-,19?,20+,21-,22-,23?,24?,25-,26?,27?,28+,29-,30?,31-,33?,34-,35?,36-/m1/s1

612069-27-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3'-N,N-Di(desmethyl) Azithromycin

1.2 Other means of identification

Product number -
Other names (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-11-[(2S,3R,4S,6R)-4-amino-3-hydroxy-6-methyloxan-2-yl]oxy-2-ethyl-3,4,10-trihydroxy-13-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,6,8,10,12,14-heptamethyl-1-oxa-6-azacyclopentadecan-15-one

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:612069-27-9 SDS

612069-27-9Downstream Products

612069-27-9Relevant articles and documents

Macrocyclic lactone impurity synthetic method

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Paragraph 0030; 0031, (2017/04/28)

The invention relates to a method for preparing an azithromycin impurity I and an azithromycin impurity E. The method comprises the following steps: mixing azithromycin with a solvent, and adding the mixture into a compound which is shown as (I) in the description to perform a demethylation reaction, wherein R1 and R2 are respectively and independently methyl, ethyl, propyl, naphthenic group, a phenyl and p-methylphenyl. According to the method for preparing azithromycin impurity, the reaction is carried out under a mild condition; the method can be used for preparing the azithromycin impurity I and the azithromycin impurity E by controlling the amount of a reagent; the HPLC purity of the azithromycin impurities prepared by the method is 98 percent or more.

Novel desosamine-modified 14- and 15-membered macrolides without antibacterial activity

Jakopovi?, Ivana Palej,Kraja?i?, Mirjana Bukvi?,?kugor, Maja Matanovi?,?timac, Vlado,Pe?i?, Dijana,Vujasinovi?, Ines,Alihod?i?, Sulejman,Paljetak, Hana ?ip?i?,Kragol, Goran

, p. 3527 - 3530 (2012/07/03)

Novel modifications of the desosamine sugar of 14- and 15-membered antibacterial macrolides, in which the desosamine was fused with N-substituted-1,3-oxazolidin-2-ones, were developed in order to completely suppress antibacterial activity and make them pr

Derivatives of azithromycin

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Page/Page column 4, (2008/06/13)

The invention relates to derivatives of azithromycin, processes for the manufacture thereof and pharmaceutical compositions thereof preferably together with azithromycin.

BIFUNCTIONAL HETEROCYCLIC COMPOUNDS AND METHODS OF MAKING AND USING SAME

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Page/Page column 310; 311, (2010/02/06)

The invention provides a family of bifunctional heterocyclic compounds useful as anti-infective, anti-proliferative, anti-inflammatory, and prokinetic agents. The invention also provides methods of making the bifunctional hetercyclic compounds, and methods of using such compounds as anti-infective, anti-proliferative agents, anti-inflammatory, and/or prokinetic agents.

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