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Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate

  • Product Name Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate
  • cas 40922-77-8
  • purity 99%
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1.What is the Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate ?

Antibacterial.

2.What is the CAS number for Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate ?

The CAS number of Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate is 40922-77-8.

More information of Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate 40922-77-8 are:

CAS?Number

40922-77-8

Density

1.19 g/cm3

Boiling Point

887.2 °C at 760 mmHg

Flash Point

490.3 °C

Vapor Pressure

0mmHg at 25°C

Refractive Index

1.528

PSA

212.12000

LogP

3.97430

Pka

13.06±0.70(Predicted)

3.What are another words for Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate ?

Synonyms?for?Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate 40922-77-8:Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate;10-Propionyljosamycin;9-Propionyljosamycin;UNII-053VA4B06Y;6-{[6-{[(11Z)-4-(Acetyloxy)-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-10-(propanoyloxy)oxacyclohexadeca-11,13-dien-6-yl]oxy}-4-(dimethylamino)-5-hydroxy-2-methyltetrahydro-2H-pyran-3-yl]oxy}-4-hydr oxy-2,4-dimethyltetrahydro-2H-pyran-3-yl 3-methylbutanoate;

4.What is the molecular formula of Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate?

The chemical formula of ?Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate is?C45H73NO16 which containing 45 Carbon atoms,73 Hydrogen atoms,1 Nitrogen atoms and 16 Oxygen atoms,and the molecular weight of??Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate?is 884.0582.

5.What is Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate (40922-77-8) used for?

Leucomycin V, 3-acetate 4B-(3-methylbutanoate) 9-propanoate is a semi-synthetic macrolide antibiotic derived from the natural macrolide leucomycin. It is characterized by the presence of an acetyl group at the 3-position, a 3-methylbutanoate group at the 4B-position, and a propanoate group at the 9-position. These structural modifications enhance its antibacterial properties and broaden its spectrum of activity.

InChI:InChI=1/C45H73NO16/c1-13-34(49)59-32-18-16-14-15-17-27(5)55-36(51)23-33(58-30(8)48)42(54-12)41(31(19-20-47)22-26(32)4)62-44-39(52)38(46(10)11)40(28(6)57-44)61-37-24-45(9,53)43(29(7)56-37)60-35(50)21-25(2)3/h14-16,18,20,25-29,31-33,37-44,52-53H,13,17,19,21-24H2,1-12H3/b15-14-,18-16-

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