Cas 1355640-88-8,(2E,6E,10E)-1-tert-butyldiphenylsiloxy-14-bromo-15-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10-triene

1355640-88-8

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Basic information

Product Name: (2E,6E,10E)-1-tert-butyldiphenylsiloxy-14-bromo-15-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10-triene
Synonyms: (2E,6E,10E)-1-tert-butyldiphenylsiloxy-14-bromo-15-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10-triene
CAS NO:1355640-88-8
Molecular Formula:
Molecular Weight: 625.805
EINECS: N/A
Product Categories: N/A
Mol File: 1355640-88-8.mol
Article Data: 1

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: (2E,6E,10E)-1-tert-butyldiphenylsiloxy-14-bromo-15-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10-triene(CAS DataBase Reference)
NIST Chemistry Reference: (2E,6E,10E)-1-tert-butyldiphenylsiloxy-14-bromo-15-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10-triene(1355640-88-8)
EPA Substance Registry System: (2E,6E,10E)-1-tert-butyldiphenylsiloxy-14-bromo-15-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10-triene(1355640-88-8)

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: 1355640-88-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1355640-88-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,5,6,4 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1355640-88:
(9*1)+(8*3)+(7*5)+(6*5)+(5*6)+(4*4)+(3*0)+(2*8)+(1*8)=168
168 % 10 = 8
So 1355640-88-8 is a valid CAS Registry Number.

1355640-88-8Upstream product

1355640-88-8Downstream Products

1355640-89-9 (2E,6E,10E)-1-tert-butyldiphenylsiloxy-14,15-epoxy-3,7,11,15-tetramethylhexadeca-2,6,10-triene

1355640-88-8Relevant articles and documents

Biomimetic cyclization of epoxide precursors of indole mono-, sesquiand diterpene alkaloids by lewis acids

Isaka, Tetsuya,Hasegawa, Morifumi,Toshima, Hiroaki

, p. 2213 - 2222 (2011)

Cyclization of the synthesized epoxide precursors of indole mono-, sesqui- and diterpene alkaloids was performed to elucidate the mechanism for biomimetic cationic cyclization to polycyclic structures. 3-(6,7- Epoxygeranyl)indole (11), 3-(10,11-epoxyfarne

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