Leucomycin A1

Modify Date: 2025-08-31 15:37:51

Leucomycin A1 Structure
Leucomycin A1 structure
Common Name Leucomycin A1
CAS Number 16846-34-7 Molecular Weight 785.96
Density 1.21g/cm3 Boiling Point 874.7ºC at 760 mmHg
Molecular Formula C40H67NO14 Melting Point N/A
MSDS N/A Flash Point 482.8ºC

 Use of Leucomycin A1


Leucomycin A1 is a main component of the leucomycin complex produced by Streptomyces kitasatoensis, Leucomycin A1 is an antibiotic[1].

 Names

Name Leucomycin-A1
Synonym More Synonyms

 Leucomycin A1 Biological Activity

Description Leucomycin A1 is a main component of the leucomycin complex produced by Streptomyces kitasatoensis, Leucomycin A1 is an antibiotic[1].
Related Catalog
References

[1]. Watanabe T, et al. Studies on leucomycin. V. Isolation of mycaros-4-isovalerate from leucomycin A1. Bulletin of the Chemical Society of Japan, 1961, 34(9): 1285-1288.

 Chemical & Physical Properties

Density 1.21g/cm3
Boiling Point 874.7ºC at 760 mmHg
Molecular Formula C40H67NO14
Molecular Weight 785.96
Flash Point 482.8ºC
Exact Mass 785.45600
PSA 199.98000
LogP 2.44260
Vapour Pressure 0mmHg at 25°C
Index of Refraction 1.541

 Synonyms

Leucomycin V,3,4(sup B)-diacetate
Turimycin A2
Leucomycin A8
Leukomycin A8
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here


Get all suppliers and price by the below link:

Leucomycin A1 suppliers

Leucomycin A1 price

Related Compounds: More...
Leucomycin A1
1392-21-8
Leucomycin A13
78897-52-6
Leucomycin V, 9-(ethyl carbonate) 3,4B-dipropanoate
62646-55-3
Leucomycin V, 2,3-dihydro-12,13-epoxy-12,13-dihydro-, 4B-acetate 3-propanoate
65947-11-7
Leucomycin V, 4(sup B),9-diacetate 3-propanoate
65178-01-0
Leucomycin A4
18361-46-1
[6-[4-(dimethylamino)-5-hydroxy-6-[[(14E)-8-methoxy-3,12-dimethyl-5-oxo-10-(2-oxoethyl)-7,13-di(propanoyloxy)-4,17-dioxabicyclo[14.1.0]heptadec-14-en-9-yl]oxy]-2-methyloxan-3-yl]oxy-4-hydroxy-2,4-dimethyloxan-3-yl] 3-methylbutanoate
35775-65-6
[(14E)-9-[4-(dimethylamino)-3-hydroxy-5-(4-hydroxy-4,6-dimethyl-5-propanoyloxyoxan-2-yl)oxy-6-methyloxan-2-yl]oxy-8-methoxy-3,12-dimethyl-5-oxo-10-(2-oxoethyl)-13-propanoyloxy-4,17-dioxabicyclo[14.1.0]heptadec-14-en-7-yl] propanoate
35775-84-9
Leucomycin V,9-deoxy-12,13-epoxy-12,13-dihydro-9-oxo-, 3-acetate 4B-(3-methylbutanoate),(12S,13S)-
4564-87-8
4-Amino-2-bromonaphthalen-1-ol
2060063-47-8
Na(2)a(2)-(2-Phenylethyl)-N-(phenylmethyl)imidodicarbonimidic diamide
1309598-58-0
3-(3-(5-(2-Methoxyethoxy)pyrimidin-2-yl)benzyl)-1-(1-methyl-1h-pyrazol-4-yl)pyridazin-4(1h)-one
1314380-61-4
3-(3-(5-Methoxypyrimidin-2-yl)benzyl)-1-(1-methyl-1h-pyrazol-4-yl)pyridazin-4(1h)-one
1314380-62-5
Ethyl 2-(3-oxocyclobutyl)acetate
145822-90-8
(1,3,3-Trimethylcyclobutyl)methanamine
1526515-03-6
1-(1-Methylpyrazol-4-yl)-3-[[3-(5-methyl-1,3-thiazol-2-yl)phenyl]methyl]pyridazin-4-one
1314380-76-1
5-[[1-(1-methylpyrazol-4-yl)-4-oxopyridazin-3-yl]methyl]-3H-1,3-benzoxazol-2-one
1314380-81-8
Methyl 3-hydroxythieno[3,2-b]thiophene-2-carboxylate
177974-13-9
3-((cyclopropylmethyl)thio)-4-methyl-4H-1,2,4-triazole
917383-06-3