Cas 1303559-48-9,2-((tetrahydro-4-phenylfuran-2-yl)methyl)-2-(4-methylpenta-2,3-dienyl)-malonic acid dimethyl ester

1303559-48-9

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Basic information

Product Name: 2-((tetrahydro-4-phenylfuran-2-yl)methyl)-2-(4-methylpenta-2,3-dienyl)-malonic acid dimethyl ester
Synonyms: 2-((tetrahydro-4-phenylfuran-2-yl)methyl)-2-(4-methylpenta-2,3-dienyl)-malonic acid dimethyl ester
CAS NO:1303559-48-9
Molecular Formula:
Molecular Weight: 372.461
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: 2-((tetrahydro-4-phenylfuran-2-yl)methyl)-2-(4-methylpenta-2,3-dienyl)-malonic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-((tetrahydro-4-phenylfuran-2-yl)methyl)-2-(4-methylpenta-2,3-dienyl)-malonic acid dimethyl ester(1303559-48-9)
EPA Substance Registry System: 2-((tetrahydro-4-phenylfuran-2-yl)methyl)-2-(4-methylpenta-2,3-dienyl)-malonic acid dimethyl ester(1303559-48-9)

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: 1303559-48-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1303559-48-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,3,5,5 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1303559-48:
(9*1)+(8*3)+(7*0)+(6*3)+(5*5)+(4*5)+(3*9)+(2*4)+(1*8)=139
139 % 10 = 9
So 1303559-48-9 is a valid CAS Registry Number.

1303559-48-9Upstream product

1303559-48-9Downstream Products

1303559-75-2 dimethyl 4,5,8,9-tetrahydro-1,1-dimethyl-4-phenylbenzo[c]oxepine-7,7(1H,3H,6H)-dicarboxylate

1303559-48-9Relevant academic research and scientific papers

Gold and bronsted acid catalyzed hydride shift onto allenes: Divergence in product selectivity

Bolte, Benoit,Gagosz, Fabien

supporting information; experimental part, p. 7696 - 7699 (2011/06/27)

A series of allenyl ethers can be transformed into various fused or spiro tetrahydrofurans and tetrahydropyrans following a hydride shift/cyclization sequence. A divergence in product selectivity, which depends on the nature of the catalyst used (Au(I) complex or Bronsted acid), was observed.

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