Cas 1585173-63-2,spiro[5'.3]oxindolespiro[6'.16]-7'-(3,4-dimethoxyphenyl)tetrahydro-1H-pyrrolo[1',2'-c][1',3']thiazoloestrone

1585173-63-2

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Basic information

Product Name: spiro[5'.3]oxindolespiro[6'.16]-7'-(3,4-dimethoxyphenyl)tetrahydro-1H-pyrrolo[1',2'-c][1',3']thiazoloestrone
Synonyms: spiro[5'.3]oxindolespiro[6'.16]-7'-(3,4-dimethoxyphenyl)tetrahydro-1H-pyrrolo[1',2'-c][1',3']thiazoloestrone
CAS NO:1585173-63-2
Molecular Formula:
Molecular Weight: 636.812
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]oxindolespiro[6'.16]-7'-(3,4-dimethoxyphenyl)tetrahydro-1H-pyrrolo[1',2'-c][1',3']thiazoloestrone(CAS DataBase Reference)
NIST Chemistry Reference: spiro[5'.3]oxindolespiro[6'.16]-7'-(3,4-dimethoxyphenyl)tetrahydro-1H-pyrrolo[1',2'-c][1',3']thiazoloestrone(1585173-63-2)
EPA Substance Registry System: spiro[5'.3]oxindolespiro[6'.16]-7'-(3,4-dimethoxyphenyl)tetrahydro-1H-pyrrolo[1',2'-c][1',3']thiazoloestrone(1585173-63-2)

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: 1585173-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1585173-63-2 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, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1585173-63:
(9*1)+(8*5)+(7*8)+(6*5)+(5*1)+(4*7)+(3*3)+(2*6)+(1*3)=192
192 % 10 = 2
So 1585173-63-2 is a valid CAS Registry Number.

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1585173-63-2Relevant 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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