Cas 915975-68-7,4,12-Dioxa-3,13-disilapentadeca-6,7-diene, 2,2,8,13,13,14,14-heptamethyl-3,3-diphenyl-5-[4-(trimethylsilyl)-3-butyn- 1-yl]-

915975-68-7

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Basic information

Product Name: 4,12-Dioxa-3,13-disilapentadeca-6,7-diene, 2,2,8,13,13,14,14-heptamethyl-3,3-diphenyl-5-[4-(trimethylsilyl)-3-butyn- 1-yl]-
Synonyms:
CAS NO:915975-68-7
Molecular Formula: C37H58O2Si3
Molecular Weight: 619.123
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: 4,12-Dioxa-3,13-disilapentadeca-6,7-diene, 2,2,8,13,13,14,14-heptamethyl-3,3-diphenyl-5-[4-(trimethylsilyl)-3-butyn- 1-yl]-(CAS DataBase Reference)
NIST Chemistry Reference: 4,12-Dioxa-3,13-disilapentadeca-6,7-diene, 2,2,8,13,13,14,14-heptamethyl-3,3-diphenyl-5-[4-(trimethylsilyl)-3-butyn- 1-yl]-(915975-68-7)
EPA Substance Registry System: 4,12-Dioxa-3,13-disilapentadeca-6,7-diene, 2,2,8,13,13,14,14-heptamethyl-3,3-diphenyl-5-[4-(trimethylsilyl)-3-butyn- 1-yl]-(915975-68-7)

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: 915975-68-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 915975-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,9,7 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 915975-68:
(8*9)+(7*1)+(6*5)+(5*9)+(4*7)+(3*5)+(2*6)+(1*8)=217
217 % 10 = 7
So 915975-68-7 is a valid CAS Registry Number.

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915975-68-7Relevant academic research and scientific papers

The allenic Alder-ene reaction: constitutional group selectivity and its application to the synthesis of ovalicin

Brummond, Kay M.,McCabe, Jamie M.

, p. 10541 - 10554 (2007/10/03)

The scope of the novel allenic Alder-ene reaction using Rh(I) and Ir(I) catalysts has been extended to differentially substituted 1,1,3-trisubstituted allenes. This allenyl substitution pattern can give three possible cross-conjugated triene products. The

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