Cas 1314045-41-4,1-chloro-3-(1-(4-methoxyphenyl)-3-phenylprop-2-ynyloxy)-2-methylbenzene

1314045-41-4

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Basic information

Product Name: 1-chloro-3-(1-(4-methoxyphenyl)-3-phenylprop-2-ynyloxy)-2-methylbenzene
Synonyms: 1-chloro-3-(1-(4-methoxyphenyl)-3-phenylprop-2-ynyloxy)-2-methylbenzene
CAS NO:1314045-41-4
Molecular Formula:
Molecular Weight: 362.856
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: 1-chloro-3-(1-(4-methoxyphenyl)-3-phenylprop-2-ynyloxy)-2-methylbenzene(CAS DataBase Reference)
NIST Chemistry Reference: 1-chloro-3-(1-(4-methoxyphenyl)-3-phenylprop-2-ynyloxy)-2-methylbenzene(1314045-41-4)
EPA Substance Registry System: 1-chloro-3-(1-(4-methoxyphenyl)-3-phenylprop-2-ynyloxy)-2-methylbenzene(1314045-41-4)

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: 1314045-41-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1314045-41-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,0,4 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1314045-41:
(9*1)+(8*3)+(7*1)+(6*4)+(5*0)+(4*4)+(3*5)+(2*4)+(1*1)=104
104 % 10 = 4
So 1314045-41-4 is a valid CAS Registry Number.

1314045-41-4Upstream product

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1314045-41-4Relevant academic research and scientific papers

A DDQ-promoted metal-free cross-coupling of 1,3-diarylpropynes with hydroxyl via Sp3 C-H bond activation to form C-O bond

Mo, Hanjie,Bao, Weiliang

supporting information; experimental part, p. 4793 - 4799 (2011/07/31)

A metal-free coupling reaction between 1,3-diarylpropynes and alcohols/phenols/acids via propargylic sp3 C-H bonds activation and C-O bond formation reaction promoted by DDQ was realized. The reaction afforded series of propargyl ethers, propargyl esters and propargyl ketals.

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