Cas 1313370-75-0,methyl 1-(4-bromophenyl)-2-methyl-3-(prop-1-yn-1-yl)cycloprop-2-enecarboxylate

1313370-75-0

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Basic information

Product Name: methyl 1-(4-bromophenyl)-2-methyl-3-(prop-1-yn-1-yl)cycloprop-2-enecarboxylate
Synonyms: methyl 1-(4-bromophenyl)-2-methyl-3-(prop-1-yn-1-yl)cycloprop-2-enecarboxylate
CAS NO:1313370-75-0
Molecular Formula:
Molecular Weight: 305.171
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 1-(4-bromophenyl)-2-methyl-3-(prop-1-yn-1-yl)cycloprop-2-enecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 1-(4-bromophenyl)-2-methyl-3-(prop-1-yn-1-yl)cycloprop-2-enecarboxylate(1313370-75-0)
EPA Substance Registry System: methyl 1-(4-bromophenyl)-2-methyl-3-(prop-1-yn-1-yl)cycloprop-2-enecarboxylate(1313370-75-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1313370-75-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1313370-75-0 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, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1313370-75:
(9*1)+(8*3)+(7*1)+(6*3)+(5*3)+(4*7)+(3*0)+(2*7)+(1*5)=120
120 % 10 = 0
So 1313370-75-0 is a valid CAS Registry Number.

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1313370-75-0Relevant 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.

supporting information; experimental part, p. 3984 - 3987 (2011/09/16)

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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