Cas 1422584-48-2,4-[(1E)-3-(1-benzofuran-2-yl)-3-oxoprop-1-en-1-yl]-2-methoxyphenyl chloroacetate

1422584-48-2

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Basic information

Product Name: 4-[(1E)-3-(1-benzofuran-2-yl)-3-oxoprop-1-en-1-yl]-2-methoxyphenyl chloroacetate
Synonyms: 4-[(1E)-3-(1-benzofuran-2-yl)-3-oxoprop-1-en-1-yl]-2-methoxyphenyl chloroacetate
CAS NO:1422584-48-2
Molecular Formula:
Molecular Weight: 370.789
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: 4-[(1E)-3-(1-benzofuran-2-yl)-3-oxoprop-1-en-1-yl]-2-methoxyphenyl chloroacetate(CAS DataBase Reference)
NIST Chemistry Reference: 4-[(1E)-3-(1-benzofuran-2-yl)-3-oxoprop-1-en-1-yl]-2-methoxyphenyl chloroacetate(1422584-48-2)
EPA Substance Registry System: 4-[(1E)-3-(1-benzofuran-2-yl)-3-oxoprop-1-en-1-yl]-2-methoxyphenyl chloroacetate(1422584-48-2)

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: 1422584-48-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1422584-48-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,2,5,8 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1422584-48:
(9*1)+(8*4)+(7*2)+(6*2)+(5*5)+(4*8)+(3*4)+(2*4)+(1*8)=152
152 % 10 = 2
So 1422584-48-2 is a valid CAS Registry Number.

1422584-48-2Upstream product

79-04-9 chloroacetyl chloride

1422584-48-2Downstream Products

1422584-48-2Relevant academic research and scientific papers

Synthesis of some acylated 2-pyrazoline and chalcone derivatives

Coskun, Demet,Ahmedzade, Misir

, p. 1193 - 1199 (2014)

α-Haloesters containing the chalcone structure and α-haloamides containing the pyrazoline ring have been synthesized by reaction of substituted hydroxy chalcones and pyrazoline derivatives (prepared as reported elsewhere; J Chem 8(4):1574-1581, 2011) with

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