Cas 119760-43-9,3,5-Dinitro-benzoic acid (3aR,6R,8aS,9R)-(octahydro-3a,6-methano-azulen-9-yl) ester

119760-43-9

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Basic information

Product Name: 3,5-Dinitro-benzoic acid (3aR,6R,8aS,9R)-(octahydro-3a,6-methano-azulen-9-yl) ester
Synonyms:
CAS NO:119760-43-9
Molecular Formula:
Molecular Weight: 360.367
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: 3,5-Dinitro-benzoic acid (3aR,6R,8aS,9R)-(octahydro-3a,6-methano-azulen-9-yl) ester(CAS DataBase Reference)
NIST Chemistry Reference: 3,5-Dinitro-benzoic acid (3aR,6R,8aS,9R)-(octahydro-3a,6-methano-azulen-9-yl) ester(119760-43-9)
EPA Substance Registry System: 3,5-Dinitro-benzoic acid (3aR,6R,8aS,9R)-(octahydro-3a,6-methano-azulen-9-yl) ester(119760-43-9)

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: 119760-43-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 119760-43-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,7,6 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 119760-43:
(8*1)+(7*1)+(6*9)+(5*7)+(4*6)+(3*0)+(2*4)+(1*3)=139
139 % 10 = 9
So 119760-43-9 is a valid CAS Registry Number.

119760-43-9Upstream product

119760-43-9Downstream Products

119760-43-9Relevant academic research and scientific papers

Solvolytic Rearrangement of 5,6-Polymethylenebicyclooctan-2-ol Derivatives to Functionalized Polymethylenebicyclo- and octanes

Ue, Masaki,Nagashima, Teruhisa,Kinugawa, Masahiko,Kakiuchi, Kiyomi,Tobe, Yoshito,et. al.

, p. 1521 - 1522 (1988)

The functionalized polymethylenebicyclo- and octane derivatives are newly synthesized from endo- and exo-5,6-polymethylenebicyclooct-2-yl 3,5-dinitrobenzoates by skeletal rearrangement using solvolysis.

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