Cas 39003-20-8,(5Z,11α,13E,15S)-9-Oxo-11,15-bis[(trimethylsilyl)oxy]prosta-5,13-dien-1-oic acid trimethylsilyl ester

39003-20-8

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Basic information

Product Name: (5Z,11α,13E,15S)-9-Oxo-11,15-bis[(trimethylsilyl)oxy]prosta-5,13-dien-1-oic acid trimethylsilyl ester
Synonyms: (5Z,11α,13E,15S)-9-Oxo-11,15-bis[(trimethylsilyl)oxy]prosta-5,13-dien-1-oic acid trimethylsilyl ester
CAS NO:39003-20-8
Molecular Formula: C29H56O5Si3
Molecular Weight: 569.00844
EINECS: N/A
Product Categories: N/A
Mol File: 39003-20-8.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (5Z,11α,13E,15S)-9-Oxo-11,15-bis[(trimethylsilyl)oxy]prosta-5,13-dien-1-oic acid trimethylsilyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (5Z,11α,13E,15S)-9-Oxo-11,15-bis[(trimethylsilyl)oxy]prosta-5,13-dien-1-oic acid trimethylsilyl ester(39003-20-8)
EPA Substance Registry System: (5Z,11α,13E,15S)-9-Oxo-11,15-bis[(trimethylsilyl)oxy]prosta-5,13-dien-1-oic acid trimethylsilyl ester(39003-20-8)

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: 39003-20-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 39003-20-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,0 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39003-20:
(7*3)+(6*9)+(5*0)+(4*0)+(3*3)+(2*2)+(1*0)=88
88 % 10 = 8
So 39003-20-8 is a valid CAS Registry Number.

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39003-20-8Relevant articles and documents

Prostaglandin fluorides in synthesis of natural prostaglandin derivatives at carboxyl group

Serkov,Bezuglov

experimental part, p. 111 - 117 (2009/08/15)

Methods of synthesis of prostaglandin fluorides were developed and their properties were investigated. These compounds were shown to be convenient synthetic precursors for obtaining esters and amides of natural prostaglandins and their fluorodeoxy analogu

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