Cas 83864-79-3,5-propyl-3-(4-propylphenoxy)benzene-1,2-diol

83864-79-3

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Basic information

Product Name: 5-propyl-3-(4-propylphenoxy)benzene-1,2-diol
Synonyms: 5-propyl-3-(4-propylphenoxy)benzene-1,2-diol
CAS NO:83864-79-3
Molecular Formula:
Molecular Weight: 286.371
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: 5-propyl-3-(4-propylphenoxy)benzene-1,2-diol(CAS DataBase Reference)
NIST Chemistry Reference: 5-propyl-3-(4-propylphenoxy)benzene-1,2-diol(83864-79-3)
EPA Substance Registry System: 5-propyl-3-(4-propylphenoxy)benzene-1,2-diol(83864-79-3)

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: 83864-79-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 83864-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,6 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83864-79:
(7*8)+(6*3)+(5*8)+(4*6)+(3*4)+(2*7)+(1*9)=173
173 % 10 = 3
So 83864-79-3 is a valid CAS Registry Number.

83864-79-3Upstream product

83864-78-2 obovatol

83864-79-3Downstream Products

1146930-84-8 3-(4-propylphenoxy)-2-methoxy-5-propylphenol

83864-79-3Relevant academic research and scientific papers

JJK694, a synthesized obovatol derivative, inhibits platelet activation by suppressing cyclooxygenase and lipoxygenase activities

Yu, Ji-Yeon,Lee, Jung-Jin,Jung, Jae-Kyung,Min, Yong-Ki,Kim, Tack-Joong,Ma, Jin Yeul,Lee, Mi-Yea,Yun, Yeo-Pyo

, p. 2038 - 2043 (2012)

Obovatol has various biological activities, including anti-proliferative, neurotrophic, anti-fibrillogenic, antiplatelet, anti-fungal and anti-inflammatory activities. In this study, we investigated the effects of JJK694, a synthesized obovatol derivative

Synthesis and anti-platelet activity of obovatol derivatives

Kwak, Jae-Hwan,Lee, Seul,Park, Eun-Seok,In, Jin-Kyung,Song, Jiho,Kim, Young Jin,Choi, Nam Song,Lee, Heesoon,Yun, Yeo-Pyo,Hong, Jin Tae,Kwak, Young-Shin,Min, Kyung Hoon,Jung, Jae-Kyung

experimental part, p. 1107 - 1112 (2012/08/07)

Obovatol derivatives were synthesized and evaluated for anti-platelet activity. Three derivatives (1, 2, 4i) displayed equipotent activity to obovatol in arachidonic acid-induced platelet aggregation. An initial SAR study revealed that the introduction of alkoxy group in B ring could enhance inhibitory activity.

Novel obovatol derivatives or pharmaceutically acceptable salts thereof, preparation method thereof and pharmaceutical composition for the prevention and treatment of cancer containing the same as an active ingredient

-

Page/Page column 5, (2009/10/01)

Disclosed herein are novel obovatol derivatives represented by Chemical Formula 1, and pharmaceutically acceptable salts thereof. Having the ability to inhibit the growth of cancer cells and induce apoptosis in cancer cells, the derivatives or pharmaceuti

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