Cas 121682-08-4,1,4-Dimethyl-3-oxa-6,7-diaza-tricyclo[3.3.0.0<sup>2,4</sup>]octane-6,7-dicarboxylic acid 7-benzyl ester 6-ethyl ester

121682-08-4

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Basic information

Product Name: 1,4-Dimethyl-3-oxa-6,7-diaza-tricyclo[3.3.0.0^2,4]octane-6,7-dicarboxylic acid 7-benzyl ester 6-ethyl ester
Synonyms: 1,4-Dimethyl-3-oxa-6,7-diaza-tricyclo[3.3.0.0^2,4]octane-6,7-dicarboxylic acid 7-benzyl ester 6-ethyl ester
CAS NO:121682-08-4
Molecular Formula:
Molecular Weight: 346.383
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: 1,4-Dimethyl-3-oxa-6,7-diaza-tricyclo[3.3.0.0^2,4]octane-6,7-dicarboxylic acid 7-benzyl ester 6-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1,4-Dimethyl-3-oxa-6,7-diaza-tricyclo[3.3.0.0^2,4]octane-6,7-dicarboxylic acid 7-benzyl ester 6-ethyl ester(121682-08-4)
EPA Substance Registry System: 1,4-Dimethyl-3-oxa-6,7-diaza-tricyclo[3.3.0.0^2,4]octane-6,7-dicarboxylic acid 7-benzyl ester 6-ethyl ester(121682-08-4)

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: 121682-08-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 121682-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,8 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 121682-08:
(8*1)+(7*2)+(6*1)+(5*6)+(4*8)+(3*2)+(2*0)+(1*8)=104
104 % 10 = 4
So 121682-08-4 is a valid CAS Registry Number.

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121682-08-4Relevant academic research and scientific papers

Photochemical and Thermal Ring Transformations of 8-Oxa-3,4-diaza- and 3,4,8-Triazatricyclo2,6>oct-4-enes

Kurita, Jyoji,Sakai, Hiroichi,Tsuchiya, Takashi

, p. 2887 - 2896 (2007/10/02)

Photolysis of the 8-oxa-3,4-diazatricyclo2,6>oct-4-enes (17) prepared from the 1,2-diazepines (9) via five steps resulted in a ring transformation to give the 2,3-diazabicyclohex-3-enes (20), whereas the 8-aza analogues (18) gave

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