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Product Name: Butanamide, N-(5,6,7,9-tetrahydro-1,2,3, 10-tetramethyloxy-9-oxobenzo[a]heptalen-7-yl)-, (S)-
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86436-36-4

86436-36-4 structure

86436-36-4 structure

Name: Butanamide, N-(5,6,7,9-tetrahydro-1,2,3, 10-tetramethyloxy-9-oxobenzo[a]heptalen-7-yl)-, (S)-
Chemical Name: N-(1,2,3,10-tetramethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl)butanamide
CAS Number: 86436-36-4
Molecular Formula: C₂₄H₂₉NO₆
Molecular Weight: 427.49000
Create Date: 2018-06-13 19:11:52
Modify Date: 2025-09-11 06:48:40

Name	N-(1,2,3,10-tetramethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl)butanamide
Synonyms	Butanamide,N-(5,6,7,9-tetrahydro-1,2,3,10-tetramethyloxy-9-oxobenzo(a)heptalen-7-yl)-,(S) Butanamide,6,7,9-tetrahydro-1,2,3,10-tetramethyloxy-9-oxobenzo[a]heptalen-7-yl)-,(S) N-butyryldeacetylcolchicine (S)-N-(5,6,7,9-TETRAHYDRO-1,2,3,10-TETRAMETHYLOXY-9-OXOBENZO[A]HEPTALEN-7-YL)BUTANAMIDE

Density	1.22g/cm3
Boiling Point	731.5ºC at 760 mmHg
Molecular Formula	C₂₄H₂₉NO₆
Molecular Weight	427.49000
Flash Point	396.2ºC
Exact Mass	427.19900
PSA	83.09000
LogP	4.04270
Index of Refraction	1.575

CHEMICAL IDENTIFICATION

RTECS NUMBER :: ES5065000

CHEMICAL NAME :: Butyramide, N-(5,6,7,9-tetrahydro-9-oxo-1,2,3,10-tetramethoxybenz o(a)heptalen-7-yl)-, (S)-

CAS REGISTRY NUMBER :: 86436-36-4

LAST UPDATED :: 199612

DATA ITEMS CITED :: 1

MOLECULAR FORMULA :: C24-H29-N-O6

MOLECULAR WEIGHT :: 427.54

WISWESSER LINE NOTATION :: T B677 MV&T&J CO1 DO1 EO1 JMV3 NO1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intramuscular

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 2480 ug/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: JMCMAR Journal of Medicinal Chemistry. (American Chemical Soc., Distribution Office Dept. 223, POB POB 57136, West End Stn., Washington, DC 20037) V.6- 1963- Volume(issue)/page/year: 26,1365,1983

106-31-0 structure

106-31-0

3476-50-4 structure

3476-50-4

~%

86436-36-4 structure

86436-36-4

Literature: Brossi; Sharma; Atwell; Jacobson; Iorio; Molinari; Chignell Journal of Medicinal Chemistry, 1983 , vol. 26, # 10 p. 1365 - 1369

Precursor 2
106-31-0 3476-50-4
DownStream 0

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