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19275-44-6

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19275-44-6 Usage

Definition

ChEBI: An organic heterotetracyclic compound that is 3,4-dihydro-2H,12H-pyrano[2,3-a]xanthen-12-one substituted by hydroxy groups at positions 5 and 9, a methoxy group at position 10, two methyl groups at positi n 2, a prenyl group at position 11 and an oxo group at position 12.

Check Digit Verification of cas no

The CAS Registry Mumber 19275-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,7 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19275-44:
(7*1)+(6*9)+(5*2)+(4*7)+(3*5)+(2*4)+(1*4)=126
126 % 10 = 6
So 19275-44-6 is a valid CAS Registry Number.
InChI:InChI=1/C24H26O6/c1-12(2)6-7-14-19-17(11-16(26)22(14)28-5)29-18-10-15(25)13-8-9-24(3,4)30-23(13)20(18)21(19)27/h6,10-11,25-26H,7-9H2,1-5H3

19275-44-6SDS

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 1-isomangostin

1.2 Other means of identification

Product number -
Other names 5,9-dihydroxy-10-methoxy-2,2-dimethyl-11-(3-methylbut-2-enyl)-3,4-dihydropyrano[2,3-a]xanthen-12-one

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:19275-44-6 SDS

19275-44-6Upstream product

19275-44-6Downstream Products

19275-44-6Relevant articles and documents

Stout et al.

, p. 211 (1968)

Design, synthesis and structure-activity relationships of mangostin analogs as cytotoxic agents

Chi, Xiao-Qian,Zi, Cheng-Ting,Li, Hong-Mei,Yang, Liu,Lv, Yong-Feng,Li, Jin-Yu,Hou, Bo,Ren, Fu-Cai,Hu, Jiang-Miao,Zhou, Jun

, p. 41377 - 41388 (2019/01/03)

In order to better understand the structure-activity relationship of mangostin, a series of xanthone derivatives based on α-mangostin were designed and synthesized. All the compounds were evaluated for their cytotoxicity against a panel of five human canc

Bicyclomangostin: A new acid-catalysed cyclization product from mangostin

Mahabusarakam, Wilawan,Pakawatchai, Chaveng,Wiriyachitra, Pichaet,Taylor, Walter C.,Skelton, Brian W.,White, Allan H.

, p. 249 - 254 (2007/10/03)

Cyclization of mangostin with p-toluenesulfonic acid gave 1-isomangostin, 3-isomangostin, and a new cyclization product, bicyclomangostin (4). The structure of bicyclomangostin was determined by spectroscopic and X-ray crystallographic studies. The methyl ether derivatives (8) and (9) or (10) were produced on methylation of bicyclomangostin, depending on the method used.

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