Cas 697744-49-3,trifluoromethanesulfonic acid 2-(1,7,8,8a-tetrahydro-2H-naphthalen-4a-yloxymethoxy)-phenyl ester

697744-49-3

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Basic information

Product Name: trifluoromethanesulfonic acid 2-(1,7,8,8a-tetrahydro-2H-naphthalen-4a-yloxymethoxy)-phenyl ester
Synonyms: trifluoromethanesulfonic acid 2-(1,7,8,8a-tetrahydro-2H-naphthalen-4a-yloxymethoxy)-phenyl ester
CAS NO:697744-49-3
Molecular Formula:
Molecular Weight: 388.408
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: trifluoromethanesulfonic acid 2-(1,7,8,8a-tetrahydro-2H-naphthalen-4a-yloxymethoxy)-phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: trifluoromethanesulfonic acid 2-(1,7,8,8a-tetrahydro-2H-naphthalen-4a-yloxymethoxy)-phenyl ester(697744-49-3)
EPA Substance Registry System: trifluoromethanesulfonic acid 2-(1,7,8,8a-tetrahydro-2H-naphthalen-4a-yloxymethoxy)-phenyl ester(697744-49-3)

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: 697744-49-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 697744-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,7,7,4 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 697744-49:
(8*6)+(7*9)+(6*7)+(5*7)+(4*4)+(3*4)+(2*4)+(1*9)=233
233 % 10 = 3
So 697744-49-3 is a valid CAS Registry Number.

697744-49-3Upstream product

697744-49-3Downstream Products

697744-49-3Relevant academic research and scientific papers

Sequential olefin metathesis - Intramolecular asymmetric Heck reactions in the synthesis of polycycles

Laurents, Mark,Zunic, Valentin

, p. 399 - 407 (2007/10/03)

Application of the intramolecular asymmetric Heck reaction in the desymmetrization of a novel class of symmetrical bicyclodienes, synthesized through a diastereoselective double ring-closing metathesis (DSRCM) reaction, was achieved with good yields (appr

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