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**Conclusion:** 1H-Xanthene-1,8(2H)-dione, 3,4,5,6,7,9-hexahydro-9-(4-hydroxy-3-methoxyphenyl)- is a xanthenodione derivative characterized by a pyran core fused to two cyclohexen-2-one rings, forming a 1,8-dioxooctahydroxanthene scaffold. It features a 4-hydroxy-3-methoxyphenyl substituent at the 9-position and can be synthesized efficiently using green methods, such as task-specific ionic liquids or niobium pentachloride catalysis, which offer high yields and broad substrate compatibility. 1H-Xanthene-1,8(2H)-dione, 3,4,5,6,7,9-hexahydro-9-(4-hydroxy-3-methoxyphenyl)-'s structural and vibrational properties align with typical xanthenodiones, as confirmed by spectroscopic and theoretical analyses.

102159-41-1

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102159-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102159-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,5 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 102159-41:
(8*1)+(7*0)+(6*2)+(5*1)+(4*5)+(3*9)+(2*4)+(1*1)=81
81 % 10 = 1
So 102159-41-1 is a valid CAS Registry Number.

102159-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(4-hydroxy-3-methoxy-phenyl)-3,4,5,6,7,9-hexahydro-2H-xanthene-1,8-dione

1.2 Other means of identification

Product number -
Other names 9-(4-hydroxy-3-methoxyphenyl)-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H)-dione

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:102159-41-1 SDS

102159-41-1Downstream Products

102159-41-1Relevant academic research and scientific papers

Vibrational spectroscopic studies, theoretical aspects, and X-ray analysis of xanthenodiones (1,8-dioxooctahydroxanthenes)

da Silva, Milene Lopes,Teixeira, Róbson Ricardo,de Oliveira, Fabrício Marques,de Moura Guimar?es, Luciano,Martins, Felipe Terra

, p. 777 - 792 (2021)

Compounds containing a pyran moiety fused to two cyclohexen-2-one rings are collectively called xanthenodiones (1,8-dioxooctahydroxanthenes). With the aim of increasing the knowledge about the structures of xanthenodiones, in the present investigation two

A green and efficient synthesis of 9-aryl-3,4,5,6,7,9-hexahydroxanthene-1, 8-dione using a task-specific ionic liquid as dual catalyst and solvent

Ma, Jingjun,Zhou, Xin,Zang, Xiaohuan,Wang, Chun,Wang, Zhi,Li, Jingci,Li, Qing

, p. 146 - 148 (2007)

A green and efficient method for the preparation of 9-aryl-3,4,5,6,7,9- hexahydro-1H-xanthene-1,8(2H)-dione has been developed using functionalized ionic liquids as a catalyst and a reaction medium. The nature of both the counter anion and cation influenc

Facile and efficient synthesis of xanthenedione derivatives promoted by niobium pentachloride

Dos Santos, Willian H.,Da Silva-Filho, Luiz C.

, p. 1658 - 1664 (2016)

Xanthenedione derivatives were synthesised in one-pot reactions between arylaldehyde derivatives and 1, 3-cyclohexanedione promoted by niobium pentachloride. This new method is simple, cost-effective, high-yielding with a good variety of substrates genera

Alumina-sulfuric acid catalyzed eco-friendly synthesis of xanthenediones

Pramanik, Amit,Bhar, Sanjay

experimental part, p. 17 - 24 (2012/06/16)

Alumina-sulfuric acid has been developed as a cost-effective, recyclable, heterogeneous solid acid catalyst for the eco-friendly synthesis of 9-aryl-1,8-dioxododecahydroxanthenes and 9-aryl-3,3,6,6-tetramethyl-1,8- dioxooctahydroxanthenes through the cond

XANTHENEDIONE DERIVATIVES FOR THE TREATMENT OF PIGMENTATION AND SKIN AGEING DISORDERS

-

Page/Page column 15-16, (2012/02/01)

The invention relates to compound of generic formula (I) in which: R1 and R2 represent: OH, a hydrogen atom, a C1-C6 alkyl radical a C1-C6 alkoxy radical, a halogen, or OCOR3; R

CsF mediated rapid condensation of 1,3-cyclohexadione with aromatic aldehydes: Comparative study of conventional heating vs. ambient temperature

Nandre, Kamalakar P.,Patil, Vijay S.,Bhosale, Sidhanath V.

experimental part, p. 777 - 780 (2012/01/03)

A mild, efficient and high yielding protocol for the synthesis of 2,2′-arylmethelene dicyclohexane-1,3-dione derivatives at room temperature and 9-aryl-1,8-dihydrooctahydroxanthene at conventional heating using cesium fluoride as a catalyst is reported. T

Envirocat EPZ-10: A solid acid catalyst for the synthesis of 1,8-dioxo-octahydroxanthenes in aqueous medium

Pore,Shaikh,Patil,Dongare,Desai

experimental part, p. 2215 - 2219 (2010/09/18)

An efficient method for synthesis of 1,8-dioxo-octahydroxanthenes using EPZ-10 as a heterogeneous catalyst is developed. In this method, aldehydes and dimedone/cyclohexane-1,3-dione are heated at 70C in the presence of a catalytic amount of EPZ-10 in wate

Glycerol as a promoting medium for electrophilic activation of aldehydes: Catalyst-free synthesis of di(indolyl)methanes, xanthene-1,8(2H)-diones and 1-oxo-hexahydroxanthenes

He, Fei,Li, Peng,Gu, Yanlong,Li, Guangxing

experimental part, p. 1767 - 1773 (2011/02/27)

Glycerol was used, for the first time, as a green and effective promoting medium for electrophilic activation of aldehydes, and with which, a catalyst-free system for some reactions that conventionally carried out using acid catalysts, such as synthesis o

Condensation of 1,3-cyclohexanedione with aromatic aldehydes catalyzed by acidic ionic liquids

Kang, Hui,Hu, Yi,Huang, He,Wei, Ping

scheme or table, p. 223 - 227 (2009/04/14)

An efficient and convenient approach to the synthesis of 9-aryl-2, 3, 4, 5, 6, 7-hexahydro-2H-Xanthene-1, 8-dionc by condensation of 1, 3-cyclohexanedione with aromatic aldehydes catalyzed by acid ionic liquid 1-methyllimidazolium hydrogen sulphate ([Hmim

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