Cas 77270-20-3,3,5,12-trihydroxy-10-methoxy-6,11-dioxo-3-[(phenylsulfanyl)acetyl]-1,2,3,4,6,11-hexahydrotetracen-1-yl 2,3,6-trideoxy-3-[(trifluoroacetyl)amino]hexopyranoside

77270-20-3

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Basic information

Product Name: 3,5,12-trihydroxy-10-methoxy-6,11-dioxo-3-[(phenylsulfanyl)acetyl]-1,2,3,4,6,11-hexahydrotetracen-1-yl 2,3,6-trideoxy-3-[(trifluoroacetyl)amino]hexopyranoside
Synonyms:
CAS NO:77270-20-3
Molecular Formula: C₃₅H₃₂F₃NO₁₁S
Molecular Weight: 731.6889
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 894.2°C at 760 mmHg
Flash Point: 494.6°C
Appearance: N/A
Density: 1.59g/cm³
Vapor Pressure: 2.33E-34mmHg at 25°C
Refractive Index: 1.675
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3,5,12-trihydroxy-10-methoxy-6,11-dioxo-3-[(phenylsulfanyl)acetyl]-1,2,3,4,6,11-hexahydrotetracen-1-yl 2,3,6-trideoxy-3-[(trifluoroacetyl)amino]hexopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 3,5,12-trihydroxy-10-methoxy-6,11-dioxo-3-[(phenylsulfanyl)acetyl]-1,2,3,4,6,11-hexahydrotetracen-1-yl 2,3,6-trideoxy-3-[(trifluoroacetyl)amino]hexopyranoside(77270-20-3)
EPA Substance Registry System: 3,5,12-trihydroxy-10-methoxy-6,11-dioxo-3-[(phenylsulfanyl)acetyl]-1,2,3,4,6,11-hexahydrotetracen-1-yl 2,3,6-trideoxy-3-[(trifluoroacetyl)amino]hexopyranoside(77270-20-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 77270-20-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 77270-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,7 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77270-20:
(7*7)+(6*7)+(5*2)+(4*7)+(3*0)+(2*2)+(1*0)=133
133 % 10 = 3
So 77270-20-3 is a valid CAS Registry Number.

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77270-20-3Relevant academic research and scientific papers

Adriamycin Analogues. Preparation and Biological Evaluation of Some Novel 14-Thiaadriamycins

Seshadri, Ramakrishnan,Israel, Mervyn,Pegg, William J.

, p. 11 - 15 (2007/10/02)

Condensation of 14-bromodaunorubicin with thiols in methanol, in the presence of potassium carbonate, resulted in the formation of 14-thia analogues of the antitumor antibiotic adriamycin.However, similar condensation of N-(trifluoroacetyl)-14-iododaunoru

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