Cas 1173997-14-2,(5S,6S,9S)-11-(tert-butyldimethylsilyloxy)-6-(4-methoxybenzyloxy)-9-methylundec-1-en-5-ol

1173997-14-2

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Basic information

Product Name: (5S,6S,9S)-11-(tert-butyldimethylsilyloxy)-6-(4-methoxybenzyloxy)-9-methylundec-1-en-5-ol
Synonyms: (5S,6S,9S)-11-(tert-butyldimethylsilyloxy)-6-(4-methoxybenzyloxy)-9-methylundec-1-en-5-ol
CAS NO:1173997-14-2
Molecular Formula:
Molecular Weight: 450.734
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: (5S,6S,9S)-11-(tert-butyldimethylsilyloxy)-6-(4-methoxybenzyloxy)-9-methylundec-1-en-5-ol(CAS DataBase Reference)
NIST Chemistry Reference: (5S,6S,9S)-11-(tert-butyldimethylsilyloxy)-6-(4-methoxybenzyloxy)-9-methylundec-1-en-5-ol(1173997-14-2)
EPA Substance Registry System: (5S,6S,9S)-11-(tert-butyldimethylsilyloxy)-6-(4-methoxybenzyloxy)-9-methylundec-1-en-5-ol(1173997-14-2)

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: 1173997-14-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1173997-14-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,9,9 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1173997-14:
(9*1)+(8*1)+(7*7)+(6*3)+(5*9)+(4*9)+(3*7)+(2*1)+(1*4)=192
192 % 10 = 2
So 1173997-14-2 is a valid CAS Registry Number.

1173997-14-2Upstream product

1779-49-3 Methyltriphenylphosphonium bromide

1173997-14-2Downstream Products

1173997-36-8 C₃₂H₆₀O₄Si₂

1173997-14-2Relevant academic research and scientific papers

A versatile route to the tulearin class of macrolactones: synthesis of a stereoisomer of tulearin A

Mandel, Alexander L.,Bellosta, Veronique,Curran, Dennis P.,Cossy, Janine

supporting information; experimental part, p. 3282 - 3285 (2009/12/03)

A versatile synthetic approach to the tulearin class of macrolactones has been developed and deployed to make a stereoisomer of tulearin A. The knowledge gained about structure and synthesis will expedite the assignment of the stereostructure of this new

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