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Glaucarubolone is a naturally occurring quassinoid compound found in the Simaroubaceae plant family, particularly in the roots and bark of the Glaucarubin plant. It has gained attention for its potential anti-cancer properties, as it has been shown to induce apoptosis in various cancer cell lines. The compound is known for its ability to disrupt the cell cycle and inhibit the growth of cancer cells, making it a subject of interest in cancer research. Additionally, glaucarubolone has demonstrated anti-inflammatory and anti-parasitic effects, further expanding its potential therapeutic applications. However, further studies are needed to fully understand its mechanisms of action and to evaluate its safety and efficacy in clinical settings.

1990-01-8

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1990-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1990-01-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1990-01:
(6*1)+(5*9)+(4*9)+(3*0)+(2*0)+(1*1)=88
88 % 10 = 8
So 1990-01-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H26O8/c1-7-4-10(21)15(24)18(3)9(7)5-11-19-6-27-20(26,17(18)19)14(23)8(2)12(19)13(22)16(25)28-11/h4,8-9,11-15,17,22-24,26H,5-6H2,1-3H3/t8-,9+,11-,12-,13-,14-,15-,17-,18-,19+,20+/m1/s1

1990-01-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Glaucarubolone

1.2 Other means of identification

Product number -
Other names Glaucarubolon

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1990-01-8 SDS

1990-01-8Upstream product

1990-01-8Downstream Products

1990-01-8Relevant academic research and scientific papers

Synthetic studies on quassinoids: Total synthesis of (±)-glaucarubolone and (±)-holacanthone

Fleck,Grieco

, p. 1813 - 1816 (2007/10/02)

The first total synthesis of (±)-glaucarubolone (1) and (±)-holacanthone (2) is detailed which commences with tetracyclic alcohol 3.

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