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9H-Xanthene, 9-ethoxy-9-phenyl-, also known as 9-Ethoxy-9-phenyl-9H-xanthene or 9-Phenyl-9-ethoxyxanthene, is an organic compound with the molecular formula C19H16O. It is a derivative of xanthene, a tricyclic aromatic compound consisting of two benzene rings fused to a dihydropyran ring. The 9-ethoxy-9-phenyl substitution refers to the presence of an ethoxy group (-OCH2CH3) and a phenyl group (-C6H5) attached to the xanthene core at the 9th position. 9H-Xanthene, 9-ethoxy-9-phenyl- is characterized by its yellowish color and is used in various applications, including as a chemical intermediate in the synthesis of dyes and pharmaceuticals. It is important to handle 9H-Xanthene, 9-ethoxy-9-phenyl- with care due to its potential toxicity and environmental impact.

5364-39-6

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5364-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5364-39-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5364-39:
(6*5)+(5*3)+(4*6)+(3*4)+(2*3)+(1*9)=96
96 % 10 = 6
So 5364-39-6 is a valid CAS Registry Number.

5364-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-phenyl-9-ethoxyxanthene

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5364-39-6 SDS

5364-39-6Downstream Products

5364-39-6Relevant academic research and scientific papers

Some Substituted 9-Phenylxanthen-9-yl Protecting Groups

Gaffney, Piers R. J.,Changsheng, Liu,Rao, M. Vaman,Reese, Colin B.,Ward, John G.

, p. 1355 - 1360 (2007/10/02)

Xanthen-9-one 8 was converted into 9-(4-methoxyphenyl)-, 9-(4-methylphenyl)- and 9--xanthen-9-ol (10; R1 = OMe, R2 = H, 10; R1 = Me, R2 = H, and 10; R1 = H, R2 = CF3, respectively).The corresponding 5'-protected thymidine derivatives (13; R1 = OMe, R2 = H, 13; R1 = Me, R2 = H and 13; R1 = H, R2 = CF3) were obtained in satisfactory yields from thymidine 12 and the appropriate 9-chloro compounds (11; R1 = OMe, R2 = H, 11; R1 = Me, R2 = H and 11; R1 = H, R2 = CF3).In the same way, 2,7-dibromoxanthen-9-one 14 was converted into two 9-aryl-2,7-dibromoxanthen-9-ols ( compounds 15a and 15b).Reaction between thymidine 12 and the corresponding 9-chlorocompounds gave the 5'-protected thymidine derivatives 16a and 16b, also in satisfactory yields.The rates of acid-catalysed cleavage of the above five 5'-protected thymidine derivatives (13; R1 = OMe, R2 = H, 13; R1 = Me, R2 = H and 13; R1 = H, R2 = CF3), 16a and 16b were compared with those of 5'-O-(9-phenylxanthen-9-yl)thymidine 13; R1 = R2 = H and 5'-O-(triphenylmethyl)thymidine 3a; B = thymin-1-yl under the same conditions.

Synthesis and antinociceptive activity of 9-phenyl-oxy or 9-acyl-oxy derivatives of xanthene, thioxanthene and acridine

Llama, Emilio F.,Campo, Carmen del,Capo, Miguel,Anadon, Maria

, p. 391 - 396 (2007/10/02)

The synthesis of 9-alkyl-oxy or 9-acyl-oxy derivatives of xanthene, thioxanthene and acridine is reported.A potent antinociceptive activity was confirmed for the 9-phenyl-9-propionyl-oxy derivative bearing an oxygen or sulfur atom in the heteroaromatic structure. xanthene derivatives/ thioxanthene derivatives/ acridine derivatives/ trimepridine analogues/ antinociceptive activity

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