Cas 1160153-01-4,methyl 3-chloro-4,6-dihydroxy-2-(3-(6-hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)propyl)benzoate

1160153-01-4

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Basic information

Product Name: methyl 3-chloro-4,6-dihydroxy-2-(3-(6-hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)propyl)benzoate
Synonyms:
CAS NO:1160153-01-4
Molecular Formula:
Molecular Weight: 437.834
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: methyl 3-chloro-4,6-dihydroxy-2-(3-(6-hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)propyl)benzoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 3-chloro-4,6-dihydroxy-2-(3-(6-hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)propyl)benzoate(1160153-01-4)
EPA Substance Registry System: methyl 3-chloro-4,6-dihydroxy-2-(3-(6-hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)propyl)benzoate(1160153-01-4)

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: 1160153-01-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1160153-01-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,1,5 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1160153-01:
(9*1)+(8*1)+(7*6)+(6*0)+(5*1)+(4*5)+(3*3)+(2*0)+(1*1)=94
94 % 10 = 4
So 1160153-01-4 is a valid CAS Registry Number.

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1160153-01-4Relevant academic research and scientific papers

Design, synthesis, and biological evaluation of conformationally constrained cis-amide HSP90 inhibitors

Duerfeldt, Adam S.,Brandt, Gary E. L.,Blagg, Brian S.J.

, p. 2353 - 2356 (2009)

Conformationally constrained cis-amide chimeric inhibitors of Hsp90 have been synthesized and evaluated for their Hsp90 inhibitory activity. These new compounds exhibited Hsp90 ATPase inhibition and induced Hsp90-dependent client protein degradation in a

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