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119904-03-9

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  • 5-[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-13-ethyl-6,11,12-trihydroxy-3-(5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl)oxy-2,4,6,8,10,12-hexamethyl-9-(propylamino)-14-oxacyclotetradecan-1-one

    Cas No: 119904-03-9

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119904-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119904-03-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,9,0 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 119904-03:
(8*1)+(7*1)+(6*9)+(5*9)+(4*0)+(3*4)+(2*0)+(1*3)=129
129 % 10 = 9
So 119904-03-9 is a valid CAS Registry Number.
InChI:InChI=1/C40H76N2O12/c1-15-17-41-30-21(3)19-38(9,47)35(54-37-31(43)27(42(12)13)18-22(4)50-37)24(6)32(53-29-20-39(10,49-14)34(45)26(8)51-29)25(7)36(46)52-28(16-2)40(11,48)33(44)23(30)5/h21-35,37,41,43-45,47-48H,15-20H2,1-14H3

119904-03-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-(5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl)oxy-3,5,7,9,11,13-hexamethyl-10-(propylamino)-oxacyclotetradecan-2-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:119904-03-9 SDS

119904-03-9Downstream Products

119904-03-9Relevant articles and documents

Synthesis and Structure-Activity Relationships of New 9-N-Alkyl Derivatives of 9(S)-Erythromycylamine

Kirst, Herbert A.,Wind, Julie A.,Leeds, James P.,Willard, Kevin E.,Debono, Manuel,et al.

, p. 3086 - 3094 (2007/10/02)

A series of new 9-N-alkyl derivatives of 9(S)-erythromycylamine has been synthesized by reductive alkylation of erythromycylamine with aliphatic aldehydes and sodium cyanoborohydride.Alternative syntheses employing hydrogenation methods have also been dev

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