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9-ethyl-6-(octylsulfanyl)-9H-purine is a chemical compound belonging to the purine family, characterized by a unique molecular structure. It consists of a purine ring system with an ethyl group at the 9-position and an octylsulfanyl group at the 6-position. 9-ethyl-6-(octylsulfanyl)-9H-purine has potential applications in various fields, including pharmaceuticals and chemical research, due to its distinct properties and reactivity. The specific uses and effects of 9-ethyl-6-(octylsulfanyl)-9H-purine may vary depending on its interactions with other molecules and its role in different chemical processes.

15923-47-4

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15923-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15923-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,2 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15923-47:
(7*1)+(6*5)+(5*9)+(4*2)+(3*3)+(2*4)+(1*7)=114
114 % 10 = 4
So 15923-47-4 is a valid CAS Registry Number.

15923-47-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-ethyl-6-(octylthio)-9H-purine

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

More Details:15923-47-4 SDS

15923-47-4Downstream Products

15923-47-4Relevant academic research and scientific papers

Direct Sulfenylation of the Purine C8-H Bond with Thiophenols

Jiang, Wei,Zhuge, Juanping,Li, Jianxiao,Histand, Gary,Lin, Dongen

, p. 2415 - 2425 (2020/02/04)

The one-step copper-mediated regioselective formation of the C8-S bond for purine derivatives with arylthiols was achieved using air as the green oxidant in the presence of 1.0 equiv of Na2CO3 and stoichiometric CuCl and 1,10-phenanthroline monohydrate. This method provides an economical, easy-to-handle, and effective method for the synthesis of 8-sulfenylpurine derivatives in moderate to excellent yields. The reaction is selective for C8 over C2 and C6. It also tolerates a free amine on the purine, and it has a wide substrate scope.

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