Caerulomycin A

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Names

[ CAS No. ]:
21802-37-9

[ Name ]:
Caerulomycin A

[Synonym ]:
CERULOMYCIN
(E)-4-methoxy-2,2'-bipyridyl-6-aldoxime
CAERULOMYCIN A
4-Methoxy-2,2'-bipyridine-6-carbaldehyde (E)-oxime
4-Methoxy-[2,2']bipyridyl-6-carbaldehyd-(E)-oxim
Caerulomycin,Cerulomycin
(2,2'-Bipyridine)-6-carboxaldehyde,4-methoxy-,oxime,(E)
(E)-4-Methoxy-[2,2'-bipyridine]-6-carbaldehyde oxime
4-methoxy-[2,2']bipyridinyl-6-carbaldehyde oxime
4-methoxy-[2,2']bipyridyl-6-carbaldehyde-(E)-oxime
Caerulomycin A
CAERULOMYCIN

Chemical & Physical Properties

[ Density]:
1.23g/cm3

[ Boiling Point ]:
400.4ºC at 760mmHg

[ Molecular Formula ]:
C12H11N3O2

[ Molecular Weight ]:
229.23500

[ Flash Point ]:
195.9ºC

[ Exact Mass ]:
229.08500

[ PSA ]:
67.60000

[ LogP ]:
1.96030

[ Storage condition ]:
2-8℃

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301-H315-H319

[ Precautionary Statements ]:
P301 + P310-P305 + P351 + P338

[ RIDADR ]:
UN 2811 6.1 / PGIII

[ HS Code ]:
2933399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 2,2'-Bipyridine
  • 2 2'-dipyridyl-n-oxide 98
  • 4-methoxy-2,2'-bipyridine N-oxide
  • 4-Nitro-2,2'-bipyridine-N-oxide
  • caerulomycin E
  • 6-BROMO-2,2'-BIPYRIDINE N-OXIDE
  • 6-BROMO-4-METHOXY-2,2'-BIPYRIDINE
  • 6-BROMO-4-NITRO-2,2'-BIPYRIDINE-1-OXIDE

DownStream

  • 2-Picolinic acid

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

[Development of a genetic modification system for caerulomycin producer Actinoalloteichus sp. WH1-2216-6].

Wei Sheng Wu Xue Bao 51(8) , 1032-41, (2011)

In order to enable the caerulomyicn biosynthetic study by in vivo gene disruptions, it is crucial to develop a genetic modification system for the producer Actinoalloteichus sp. WH1-2216-6.The spore g...

Total synthesis of caerulomycin C via the halogen dance reaction.

Org. Lett. 4(14) , 2385-8, (2002)

[reaction: see text] The total synthesis of caerulomycin C is described. Key steps in this synthesis utilize 1,2-, 1,3-, and 1,4-halogen dance reactions for the functionalization of the pyridine ring.

Caerulomycin, an antifungal antibiotic with marked in vitro and in vivo activity against Entamoeba histolytica.

Z. Parasitenkd. 70(5) , 569-73, (1984)

The anti-amoebic action of the bipyridyl antibiotic caerulomycin was assessed in vitro and in vivo using various strains of Entamoeba histolytica from polyxenic, axenic and monoxenic cultures. Minimum...


More Articles

Related Compounds

  • caerulomycin A
  • Camellianin A
  • lactococcin A
  • maquiroside A
  • actinoplanone A
  • Influenza A virus-IN-4
  • 2-Methylbutan-2-yl sulfamate
  • methyl 1-methyl-5-(3-oxoprop-1-en-1-yl)-1H-pyrazole-4-carboxylate
  • 2-chloro-N-(1-{4H,6H,7H-thieno[3,2-c]pyran-4-yl}ethyl)pyridine-4-carboxamide
  • 5-Methyl-2-azabicyclo[2.1.1]hexane-1-carboxylic acid hydrochloride
  • 2-(Methylsulfanyl)-1,3,4-thiadiazolehydroiodide
  • 2-amino-4-(1-tert-butyl-1H-pyrazol-4-yl)-6-fluorobenzoic acid
  • 2-(4-amino-3-methyl-1H-pyrazol-1-yl)acetic acid dihydrochloride
  • 2-Amino-6-fluoro-4-[4-(trifluoromethyl)pyridin-2-yl]benzoic acid
  • 3-amino-3-(2-methyl-2H-indazol-3-yl)propanoic acid
  • 1-methyl-5-(pyrrolidin-3-yl)-1H-imidazole dihydrochloride
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