Cas 78677-92-6,(1R,4R,6S)-4-Hydroperoxy-12-oxa-tricyclo[4.4.3.0<sup>1,6</sup>]tridec-2-ene-11,13-dione

78677-92-6

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Basic information

Product Name: (1R,4R,6S)-4-Hydroperoxy-12-oxa-tricyclo[4.4.3.0^1,6]tridec-2-ene-11,13-dione
Synonyms: (1R,4R,6S)-4-Hydroperoxy-12-oxa-tricyclo[4.4.3.0^1,6]tridec-2-ene-11,13-dione
CAS NO:78677-92-6
Molecular Formula:
Molecular Weight: 238.24
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: (1R,4R,6S)-4-Hydroperoxy-12-oxa-tricyclo[4.4.3.0^1,6]tridec-2-ene-11,13-dione(CAS DataBase Reference)
NIST Chemistry Reference: (1R,4R,6S)-4-Hydroperoxy-12-oxa-tricyclo[4.4.3.0^1,6]tridec-2-ene-11,13-dione(78677-92-6)
EPA Substance Registry System: (1R,4R,6S)-4-Hydroperoxy-12-oxa-tricyclo[4.4.3.0^1,6]tridec-2-ene-11,13-dione(78677-92-6)

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: 78677-92-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78677-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,7 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78677-92:
(7*7)+(6*8)+(5*6)+(4*7)+(3*7)+(2*9)+(1*2)=196
196 % 10 = 6
So 78677-92-6 is a valid CAS Registry Number.

78677-92-6Upstream product

53295-66-2 1,2,3,4,5,8-hexahydro-naphthalene-4a,8a-dicarboxylic acid anhydride

78677-92-6Downstream Products

78677-92-6Relevant academic research and scientific papers

PROPELLANES-LIII THE -ENE REACTION OF OLEFINIC PROPELLANES WITH SINGLET OXYGEN

Landheer, Iman,Ginsburg, David

, p. 143 - 150 (1981)

The -ene reactions of propellanes containing an anhydride ring or a methylimide ring undergo secondary orbital control.In attack by 1O2 only the syn-products are obtained.In the corresponding lactone or ether steric hindrance plays a more important role in the direction of attack.

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