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54108-66-6

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54108-66-6 Usage

Structure

A derivative of caffeine with a phenylethyl group attached to the sixth position of the purine ring.

Stimulant Properties

Possesses stimulant properties similar to caffeine.

Side Effects

Potentially reduced side effects compared to caffeine.

Potential Use

Suggested as an ingredient in energy drinks and sports supplements due to its stimulating effects.

Safety and Efficacy

Further research is needed to fully understand its safety and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 54108-66-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,0 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54108-66:
(7*5)+(6*4)+(5*1)+(4*0)+(3*8)+(2*6)+(1*6)=106
106 % 10 = 6
So 54108-66-6 is a valid CAS Registry Number.

54108-66-6SDS

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 6-(2-phenylethyl)-7H-purine

1.2 Other means of identification

Product number -
Other names 6-(2-phenethyl)purine

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:54108-66-6 SDS

54108-66-6Downstream Products

54108-66-6Relevant articles and documents

Synthesis of 6-Alkylpurine Derivatives by Nickel-comlex-catalyzed Coupling Reaction of 6-(Methylthio)purine Derivatives with Grignard Reagents

Sugimura, Hideyuki,Takei, Hisashi

, p. 664 - 666 (1985)

6-(Methylthio)purine reacted with RMgX (R=C6H5, CH3(CH2)nCH2 (n=2 to 6), C6H5CH2CH2, (CH3)2C=CHCH2CH2) in the presence of 5 molpercent in refluxing THF for 8h to afford 6-aryl or 6-alkylpurines in 62-74percent yields.By applying

Substituent-directing Effect on Cytokinin Activity of the &α-Double Bond in the 6-Substituent of Purines

Nishikawa, Shiro,Kumazawa, Zenzaburo,Mizutani, Hiroyuki,Kashimura, Naoki

, p. 1089 - 1092 (2007/10/02)

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