Cas 1313370-85-2,methyl 2-methyl-1-(naphthalen-2-yl)-3-phenylcycloprop-2-enecarboxylate

1313370-85-2

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Basic information

Product Name: methyl 2-methyl-1-(naphthalen-2-yl)-3-phenylcycloprop-2-enecarboxylate
Synonyms:
CAS NO:1313370-85-2
Molecular Formula:
Molecular Weight: 314.384
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: methyl 2-methyl-1-(naphthalen-2-yl)-3-phenylcycloprop-2-enecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-methyl-1-(naphthalen-2-yl)-3-phenylcycloprop-2-enecarboxylate(1313370-85-2)
EPA Substance Registry System: methyl 2-methyl-1-(naphthalen-2-yl)-3-phenylcycloprop-2-enecarboxylate(1313370-85-2)

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: 1313370-85-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1313370-85-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,3,7 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1313370-85:
(9*1)+(8*3)+(7*1)+(6*3)+(5*3)+(4*7)+(3*0)+(2*8)+(1*5)=122
122 % 10 = 2
So 1313370-85-2 is a valid CAS Registry Number.

1313370-85-2Upstream product

591-50-4 iodobenzene

1313370-85-2Downstream Products

1313370-85-2Relevant academic research and scientific papers

Silver triflate-catalyzed cyclopropenation of internal alkynes with donor-/acceptor-substituted diazo compounds

Briones, John F.,Davies, Huw M. L.

, p. 3984 - 3987 (2011)

Silver triflate was found to be an efficient catalyst for the cyclopropenation of internal alkynes using donor-/acceptor-substituted diazo compounds as carbenoid precursors. Highly substituted cyclopropenes, which cannot be synthesized directly via rhodium(II)-catalyzed carbenoid chemistry, can now be readily accessed.

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