Cas 916895-56-2,3-methoxy-8-oxo-4,5,6,6a-tetrahydro-8H-7-oxa-benzo[4,5]cyclohepta[1,2,3-de]naphthalene-12-carboxylic acid (1-methyl-1-phenyl-ethyl)-amide

916895-56-2

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Basic information

Product Name: 3-methoxy-8-oxo-4,5,6,6a-tetrahydro-8H-7-oxa-benzo[4,5]cyclohepta[1,2,3-de]naphthalene-12-carboxylic acid (1-methyl-1-phenyl-ethyl)-amide
Synonyms:
CAS NO:916895-56-2
Molecular Formula:
Molecular Weight: 441.527
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-methoxy-8-oxo-4,5,6,6a-tetrahydro-8H-7-oxa-benzo[4,5]cyclohepta[1,2,3-de]naphthalene-12-carboxylic acid (1-methyl-1-phenyl-ethyl)-amide(CAS DataBase Reference)
NIST Chemistry Reference: 3-methoxy-8-oxo-4,5,6,6a-tetrahydro-8H-7-oxa-benzo[4,5]cyclohepta[1,2,3-de]naphthalene-12-carboxylic acid (1-methyl-1-phenyl-ethyl)-amide(916895-56-2)
EPA Substance Registry System: 3-methoxy-8-oxo-4,5,6,6a-tetrahydro-8H-7-oxa-benzo[4,5]cyclohepta[1,2,3-de]naphthalene-12-carboxylic acid (1-methyl-1-phenyl-ethyl)-amide(916895-56-2)

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: 916895-56-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 916895-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,8,9 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 916895-56:
(8*9)+(7*1)+(6*6)+(5*8)+(4*9)+(3*5)+(2*5)+(1*6)=222
222 % 10 = 2
So 916895-56-2 is a valid CAS Registry Number.

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916895-56-2Relevant academic research and scientific papers

180° unidirectional bond rotation in a biaryl lactone artificial molecular motor prototype

Dahl, Bart J.,Branchaud, Bruce P.

, p. 5841 - 5844 (2006)

(Diagram presented) A bifunctional biaryl lactone has been synthesized that should be capable of iterative unidirectional aryl-aryl bond rotation via: (1) a diastereoselective lactone ring opening, (S)-1 to (P,S)-2 or (M,S)-2; (2) a chemoselective lactoni

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