Cas 1370521-38-2,(Z)-2-[3-ethoxy-1-(4-methoxyphenyl)prop-1-en-1-yl]-4-fluoro-1-(methoxymethoxy)benzene

1370521-38-2

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Basic information

Product Name: (Z)-2-[3-ethoxy-1-(4-methoxyphenyl)prop-1-en-1-yl]-4-fluoro-1-(methoxymethoxy)benzene
Synonyms:
CAS NO:1370521-38-2
Molecular Formula:
Molecular Weight: 346.399
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: (Z)-2-[3-ethoxy-1-(4-methoxyphenyl)prop-1-en-1-yl]-4-fluoro-1-(methoxymethoxy)benzene(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-[3-ethoxy-1-(4-methoxyphenyl)prop-1-en-1-yl]-4-fluoro-1-(methoxymethoxy)benzene(1370521-38-2)
EPA Substance Registry System: (Z)-2-[3-ethoxy-1-(4-methoxyphenyl)prop-1-en-1-yl]-4-fluoro-1-(methoxymethoxy)benzene(1370521-38-2)

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: 1370521-38-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1370521-38-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,5,2 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1370521-38:
(9*1)+(8*3)+(7*7)+(6*0)+(5*5)+(4*2)+(3*1)+(2*3)+(1*8)=132
132 % 10 = 2
So 1370521-38-2 is a valid CAS Registry Number.

1370521-38-2Upstream product

474711-11-0 2-bromo-4-fluoro-1-(methoxymethoxy)benzene

1370521-38-2Downstream Products

1370521-38-2Relevant academic research and scientific papers

A one-pot three-step synthesis of Z-trisubstituted olefins from arylalkynes and their cyclization into 4-aryl-2H-chromenes

Rasolofonjatovo, Evelia,Treguier, Bret,Provot, Olivier,Hamze, Abdallah,Brion, Jean-Daniel,Alami, Mouad

, p. 1603 - 1615 (2012)

Rapid and versatile access to (Z)-trisubstituted olefins 2 and their cyclization into 4-aryl-2H-chromenes 1 starting fromarylalkynes 3 is described. In a one-pot fashion, alkynes 3 were first hydrated, then transformed into N-tosylhydrazones, and finally

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