Cas 86119-03-1,(R)-2-Methoxy-1-methyl-6-phenylsulfanyl-3,5-dihydro-4H-naphthalene-4a-carboxylic acid methyl ester

86119-03-1

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Basic information

Product Name: (R)-2-Methoxy-1-methyl-6-phenylsulfanyl-3,5-dihydro-4H-naphthalene-4a-carboxylic acid methyl ester
Synonyms: (R)-2-Methoxy-1-methyl-6-phenylsulfanyl-3,5-dihydro-4H-naphthalene-4a-carboxylic acid methyl ester
CAS NO:86119-03-1
Molecular Formula:
Molecular Weight: 342.459
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: (R)-2-Methoxy-1-methyl-6-phenylsulfanyl-3,5-dihydro-4H-naphthalene-4a-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-Methoxy-1-methyl-6-phenylsulfanyl-3,5-dihydro-4H-naphthalene-4a-carboxylic acid methyl ester(86119-03-1)
EPA Substance Registry System: (R)-2-Methoxy-1-methyl-6-phenylsulfanyl-3,5-dihydro-4H-naphthalene-4a-carboxylic acid methyl ester(86119-03-1)

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: 86119-03-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86119-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,1 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86119-03:
(7*8)+(6*6)+(5*1)+(4*1)+(3*9)+(2*0)+(1*3)=131
131 % 10 = 1
So 86119-03-1 is a valid CAS Registry Number.

86119-03-1Upstream product

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86119-03-1Relevant academic research and scientific papers

Rapid Access to a Highly Functionalized Tricyclic Bruceantin Intermediate

Pariza, R. J.,Fuchs, P. L.

, p. 2306 - 2308 (1983)

Having found several B -> (AB or BC) -> ABC ring formation strategies unsuited for the synthesis of bruceantin and other quassinoids, we have successfully produced a highly functionalized intermediate, of desired stereochemistry, from a C -> -> ABC a

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