Cas 365440-89-7,(3R,4R,5R,6S,7S,8S)-4,7-bis(p-methoxybenzoyloxy)-3,5,6,8-tetramethyl-1,9-decadiene

365440-89-7

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Basic information

Product Name: (3R,4R,5R,6S,7S,8S)-4,7-bis(p-methoxybenzoyloxy)-3,5,6,8-tetramethyl-1,9-decadiene
Synonyms: (3R,4R,5R,6S,7S,8S)-4,7-bis(p-methoxybenzoyloxy)-3,5,6,8-tetramethyl-1,9-decadiene
CAS NO:365440-89-7
Molecular Formula:
Molecular Weight: 494.628
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: (3R,4R,5R,6S,7S,8S)-4,7-bis(p-methoxybenzoyloxy)-3,5,6,8-tetramethyl-1,9-decadiene(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4R,5R,6S,7S,8S)-4,7-bis(p-methoxybenzoyloxy)-3,5,6,8-tetramethyl-1,9-decadiene(365440-89-7)
EPA Substance Registry System: (3R,4R,5R,6S,7S,8S)-4,7-bis(p-methoxybenzoyloxy)-3,5,6,8-tetramethyl-1,9-decadiene(365440-89-7)

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: 365440-89-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 365440-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,5,4,4 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 365440-89:
(8*3)+(7*6)+(6*5)+(5*4)+(4*4)+(3*0)+(2*8)+(1*9)=157
157 % 10 = 7
So 365440-89-7 is a valid CAS Registry Number.

365440-89-7Upstream product

365440-89-7Downstream Products

365440-90-0 (2R,3S,4R,5S,6R,7S)-3,6-bis(p-methoxybenzoyloxy)-2,4,5,7-tetramethyloctane-1,8-diol

365440-89-7Relevant academic research and scientific papers

Conformational analysis of meso-2,3,4,5-tetramethylhexane and some of its derivatives

Hoffmann, Reinhard W.,Menzel, Karsten

, p. 2749 - 2755 (2001)

Compounds 12-15, meso-type 2,3,4,5,6,7-hexasubstituted octane derivatives, have been synthesized using solely substrate-based asymmetric induction. Thanks to the specific relative configurations at the six stereogenic centres, these compounds have a high tendency to populate the conformation with a fully extended zig-zag backbone chain.

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