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1H-Xanthene, 2,3,4,5,6,7,8,9-octahydro-9-(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135236-30-5

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135236-30-5 Usage

Molecular structure

1H-Xanthene, 2,3,4,5,6,7,8,9-octahydro-9-(4-methoxyphenyl)has a complex molecular structure that belongs to the xanthene family of compounds.

Functional group

Contains a 4-methoxyphenyl group, which is a methoxy group (-OCH3) attached to a phenyl ring.

Industrial applications

This chemical may have various industrial applications, such as a precursor for the synthesis of organic compounds and dyes.

Pharmaceutical applications

It has potential therapeutic uses in the pharmaceutical industry, depending on the context and specific applications for which it is intended.

Customary usage

The specific properties and potential uses of this chemical would depend on the context and the specific applications for which it is intended.

Check Digit Verification of cas no

The CAS Registry Mumber 135236-30-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,2,3 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 135236-30:
(8*1)+(7*3)+(6*5)+(5*2)+(4*3)+(3*6)+(2*3)+(1*0)=105
105 % 10 = 5
So 135236-30-5 is a valid CAS Registry Number.

135236-30-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(4-methoxyphenyl)-2,3,4,5,6,7,8,9-octahydro-1H-xanthene

1.2 Other means of identification

Product number -
Other names 9-(4-methoxyphenyl)-sym-nonahydro-10-oxaanthracene

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:135236-30-5 SDS

135236-30-5Relevant academic research and scientific papers

SYNTHESIS OF 4H-PYRANS BY O-CYCLIZATION OF 1,5-DIKETONES

Blinokhvatov, A. F.,Markovtseva, O. V.,Nikolaeva, M. N.

, p. 266 - 268 (2007/10/02)

Substituted 4H-pyrans were obtained in high preparative yields by the reaction of 1,5-diketones with acetic anhydride and boron trifluoride etherate in diethyl ether.It is assumed that the heterocyclization of 1,5-diketones includes a step involving the f

3,5-DI-tert-BUTYL-o-BENZOQUINONE AS A REAGENT FOR OXIDATIVE DEHYDROGENATION OF 9R-sym-NONAHYDRO-10-CHALCOGENOANTHRACENES

Abaev, V. T.,Blinokhvatov, A. F.,Markovtseva, O. V.,Okhlobystin, O. Yu.

, p. 42 - 44 (2007/10/02)

3,5-Di-tert-butyl-o-benzoquinone is a convenient reagent for the oxidative dehydrogenation of 9R-sym-nonahydro-10-chalcogenoanthracenes.The good solubility of o-quinone itself and the corresponding pyrocatechol facilitates the isolation of the salts of 10

OXIDATIVE CLEAVAGE OF THE C-C BOND IN PROCESSES INVOLVING THE HETEROAROMATIZATION OF 9R-sym-NONAHYDRO-10-OXA(CHALCOGENA)ANTHRACENES

Blinokhvatov, A. F.,Berberova, N. T.,Archegova, A. S.,Klimov, E. S.,Shpakov, A. V.,Okhlobystin, O. Yu.

, p. 711 - 715 (2007/10/02)

The reaction of 9-(2-methoxyphenyl)- and 9-(2-thienyl)-sym-nonahydro-10-selena(thia)anthracenes with trifluoroacetic acid causes their heteroaromatization with the elimination of substituents from the γ positions of the heterorings.A similar transformatio

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