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132560-10-2

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132560-10-2 Usage

Occurrence

Found in various plants
Most notably in coffee beans, tea leaves, and cacao pods

Classification

Stimulant compound
Central nervous system stimulant
Mild diuretic

Mechanism of action

Blocks the action of adenosine
Adenosine is a neurotransmitter that relaxes the brain and makes you feel tired

Effects

Increased alertness and wakefulness

Common consumption forms

Coffee, tea, energy drinks, and soda
Also found in certain medications and supplements

Safety

Generally recognized as safe for consumption in moderate amounts

Side effects (with excessive intake)

Insomnia, nervousness, and increased heart rate

Check Digit Verification of cas no

The CAS Registry Mumber 132560-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,6 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132560-10:
(8*1)+(7*3)+(6*2)+(5*5)+(4*6)+(3*0)+(2*1)+(1*0)=92
92 % 10 = 2
So 132560-10-2 is a valid CAS Registry Number.

132560-10-2SDS

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 1-methyl-3,8-bis(2-methylpropyl)-7H-purine-2,6-dione

1.2 Other means of identification

Product number -
Other names 3,7-Dihydro-3,8-bis(2-methylpropyl)-1-methyl-1H-purine-2,6-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:132560-10-2 SDS

132560-10-2Downstream Products

132560-10-2Relevant articles and documents

Structure-activity relationships in a series of xanthine derivatives with antibronchoconstrictory and bronchodilatory activities

Merlos,Gomez,Vericat,Bartroli,Garcia-Rafanell,Forn

, p. 653 - 658 (2007/10/02)

Thirty-one 1,3,7,8-substituted xanthine derivatives have been synthesized and evaluated for bronchodilator and anti-bronchoconstrictory activities in in vitro tracheal relaxation and in vivo bronchospasm inhibition models. Activity tests have been complemented with phosphodiesterase inhibition and toxicological data. Structure-activity relationships are discussed. Compound 21 (1,3-diisobutyl-8-methylxanthine) has been selected for further pharmacological development because of its good activity profile and favourable therapeutic index, which is 14- and 38-fold greater than that of theophylline and IBMX, respectively.

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