Cas 1234514-01-2,((1R,3R)-5,9,10-trimethoxy-1-methyl-3,4-dihydro-1H-benzo[g]isochromen-3-yl)methyl 4-methylbenzenesulfonate

1234514-01-2

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Basic information

Product Name: ((1R,3R)-5,9,10-trimethoxy-1-methyl-3,4-dihydro-1H-benzo[g]isochromen-3-yl)methyl 4-methylbenzenesulfonate
Synonyms:
CAS NO:1234514-01-2
Molecular Formula:
Molecular Weight: 472.559
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: ((1R,3R)-5,9,10-trimethoxy-1-methyl-3,4-dihydro-1H-benzo[g]isochromen-3-yl)methyl 4-methylbenzenesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: ((1R,3R)-5,9,10-trimethoxy-1-methyl-3,4-dihydro-1H-benzo[g]isochromen-3-yl)methyl 4-methylbenzenesulfonate(1234514-01-2)
EPA Substance Registry System: ((1R,3R)-5,9,10-trimethoxy-1-methyl-3,4-dihydro-1H-benzo[g]isochromen-3-yl)methyl 4-methylbenzenesulfonate(1234514-01-2)

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: 1234514-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1234514-01-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,4,5,1 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1234514-01:
(9*1)+(8*2)+(7*3)+(6*4)+(5*5)+(4*1)+(3*4)+(2*0)+(1*1)=112
112 % 10 = 2
So 1234514-01-2 is a valid CAS Registry Number.

1234514-01-2Upstream product

98-59-9 p-toluenesulfonyl chloride

1234514-01-2Downstream Products

1234514-01-2Relevant academic research and scientific papers

Synthesis of triazole analogues of the nanaomycin antibiotics using 'click chemistry'

Rathwell, Kris,Sperry, Jonathan,Brimble, Margaret A.

, p. 4002 - 4009 (2010)

A series of triazole analogues of the nanaomycin family of antibiotics have been prepared using a 'click' dipolar cycloaddition of a naphthalene azide to various alkynes, followed by oxidation to the desired pyranonaphthoquinones.

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