Cas 1565804-41-2,[3S,3(1S)]-1-benzyl-3-(3-hydroxy-2-oxo-1-triethylsilyloxy-propyl)-7-iodo-3-triethylsilyloxy-1,3-dihydro-indol-2-one

1565804-41-2

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Basic information

Product Name: [3S,3(1S)]-1-benzyl-3-(3-hydroxy-2-oxo-1-triethylsilyloxy-propyl)-7-iodo-3-triethylsilyloxy-1,3-dihydro-indol-2-one
Synonyms: [3S,3(1S)]-1-benzyl-3-(3-hydroxy-2-oxo-1-triethylsilyloxy-propyl)-7-iodo-3-triethylsilyloxy-1,3-dihydro-indol-2-one
CAS NO:1565804-41-2
Molecular Formula:
Molecular Weight: 681.759
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: [3S,3(1S)]-1-benzyl-3-(3-hydroxy-2-oxo-1-triethylsilyloxy-propyl)-7-iodo-3-triethylsilyloxy-1,3-dihydro-indol-2-one(CAS DataBase Reference)
NIST Chemistry Reference: [3S,3(1S)]-1-benzyl-3-(3-hydroxy-2-oxo-1-triethylsilyloxy-propyl)-7-iodo-3-triethylsilyloxy-1,3-dihydro-indol-2-one(1565804-41-2)
EPA Substance Registry System: [3S,3(1S)]-1-benzyl-3-(3-hydroxy-2-oxo-1-triethylsilyloxy-propyl)-7-iodo-3-triethylsilyloxy-1,3-dihydro-indol-2-one(1565804-41-2)

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: 1565804-41-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1565804-41-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,5,8,0 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1565804-41:
(9*1)+(8*5)+(7*6)+(6*5)+(5*8)+(4*0)+(3*4)+(2*4)+(1*1)=182
182 % 10 = 2
So 1565804-41-2 is a valid CAS Registry Number.

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1565804-41-2Relevant academic research and scientific papers

A convergent synthesis of the fully elaborated macrocyclic core of TMC-95A

Coste, Alexis,Bayle, Alexandre,Marrot, Jerome,Evano, Gwilherm

, p. 1306 - 1309 (2014/04/03)

A concise and straightforward synthesis of the fully elaborated macrocyclic core of TMC-95A is reported. A highly efficient organocatalyzed aldolization between isatin and dihydroxyacetone derivatives and formation of the biaryl subunit with concomitant macrocyclization are the characteristic features of this synthesis.

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