Cas 1189552-21-3,2-methoxy-3-(3-methylbut-3-en-2-yl)-4-(tetrahydro-2H-pyran-2-yloxy)benzaldehyde

1189552-21-3

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Basic information

Product Name: 2-methoxy-3-(3-methylbut-3-en-2-yl)-4-(tetrahydro-2H-pyran-2-yloxy)benzaldehyde
Synonyms: 2-methoxy-3-(3-methylbut-3-en-2-yl)-4-(tetrahydro-2H-pyran-2-yloxy)benzaldehyde
CAS NO:1189552-21-3
Molecular Formula:
Molecular Weight: 304.386
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-methoxy-3-(3-methylbut-3-en-2-yl)-4-(tetrahydro-2H-pyran-2-yloxy)benzaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 2-methoxy-3-(3-methylbut-3-en-2-yl)-4-(tetrahydro-2H-pyran-2-yloxy)benzaldehyde(1189552-21-3)
EPA Substance Registry System: 2-methoxy-3-(3-methylbut-3-en-2-yl)-4-(tetrahydro-2H-pyran-2-yloxy)benzaldehyde(1189552-21-3)

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: 1189552-21-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1189552-21-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,9,5,5 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1189552-21:
(9*1)+(8*1)+(7*8)+(6*9)+(5*5)+(4*5)+(3*2)+(2*2)+(1*1)=183
183 % 10 = 3
So 1189552-21-3 is a valid CAS Registry Number.

1189552-21-3Upstream product

1189552-21-3Downstream Products

1189552-26-8 licochalcone F

1189552-21-3Relevant academic research and scientific papers

A concise synthesis of licochalcone E and its Regio-isomer, licochalcone F

Na, Younghwa,Cha, Jeong-Heon,Yoon, Ho-Geun,Kwon, Youngjoo

experimental part, p. 607 - 609 (2009/12/09)

Licochalone E is one of the retrochalcones isolated from Glycyrrhiza inflata which shows potent cytotoxicty against human tumor cell lines. Biological studies suggested that topoisomerase I inhibition correlates with cytotoxic properties. Other research r

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