Cas 1585173-30-3,spiro[5'.3]-5-chlorooxindolespiro[6'.16]-7'-(phenyl)tetrahydro-1H-pyrrolo[1',2'-c][1',3']thiazoloestrone

1585173-30-3

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Basic information

Product Name: spiro[5'.3]-5-chlorooxindolespiro[6'.16]-7'-(phenyl)tetrahydro-1H-pyrrolo[1',2'-c][1',3']thiazoloestrone
Synonyms: spiro[5'.3]-5-chlorooxindolespiro[6'.16]-7'-(phenyl)tetrahydro-1H-pyrrolo[1',2'-c][1',3']thiazoloestrone
CAS NO:1585173-30-3
Molecular Formula:
Molecular Weight: 611.205
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: spiro[5'.3]-5-chlorooxindolespiro[6'.16]-7'-(phenyl)tetrahydro-1H-pyrrolo[1',2'-c][1',3']thiazoloestrone(CAS DataBase Reference)
NIST Chemistry Reference: spiro[5'.3]-5-chlorooxindolespiro[6'.16]-7'-(phenyl)tetrahydro-1H-pyrrolo[1',2'-c][1',3']thiazoloestrone(1585173-30-3)
EPA Substance Registry System: spiro[5'.3]-5-chlorooxindolespiro[6'.16]-7'-(phenyl)tetrahydro-1H-pyrrolo[1',2'-c][1',3']thiazoloestrone(1585173-30-3)

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: 1585173-30-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1585173-30-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,5,1,7 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1585173-30:
(9*1)+(8*5)+(7*8)+(6*5)+(5*1)+(4*7)+(3*3)+(2*3)+(1*0)=183
183 % 10 = 3
So 1585173-30-3 is a valid CAS Registry Number.

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1585173-30-3Relevant academic research and scientific papers

Synthesis of novel 16-spiro steroids: 7-(Aryl)tetrahydro-1H-pyrrolo[1,2-c] [1,3]thiazolo estrone hybrid heterocycles

Jeyachandran, Veerappan,Vivek Kumar, Sundaravel,Ranjith Kumar, Raju

, p. 29 - 37 (2014/03/21)

The 1,3-dipolar cycloaddition of azomethine ylides generated in situ from the reaction of isatins or acenaphthylene-1,2-dione and 1,3-thiazolane-4- carboxylic acid to various exocyclic dipolarophiles synthesized from estrone afforded a library of novel C-

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