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1-Propyl-3-butyl-8-methylxanthine is a complex organic compound belonging to the xanthine family, which is characterized by its unique chemical structure and potential biological activities. 1-Propyl-3-butyl-8-methylxanthine is composed of a xanthine core, with a propyl group attached to the first carbon, a butyl group at the third carbon, and a methyl group at the eighth carbon. Due to its structural complexity, 1-Propyl-3-butyl-8-methylxanthine may exhibit various pharmacological properties, such as bronchodilatory, diuretic, and stimulant effects. However, its specific applications and safety profile require further investigation and research to determine its potential use in medical or industrial settings.

81250-24-0

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81250-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81250-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,5 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81250-24:
(7*8)+(6*1)+(5*2)+(4*5)+(3*0)+(2*2)+(1*4)=100
100 % 10 = 0
So 81250-24-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H20N4O2/c1-4-6-8-16-11-10(14-9(3)15-11)12(18)17(7-5-2)13(16)19/h4-8H2,1-3H3,(H,14,15)

81250-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-butyl-8-methyl-1-propyl-7H-purine-2,6-dione

1.2 Other means of identification

Product number -
Other names 1-Propyl-3-butyl-8-methylxanthine

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:81250-24-0 SDS

81250-24-0Downstream Products

81250-24-0Relevant academic research and scientific papers

Modified 3-alkyl-1,8-dibenzylxanthines as GTP-competitive inhibitors of phosphoenolpyruvate carboxykinase

Foley, Louise H.,Wang, Ping,Dunten, Pete,Ramsey, Gwendolyn,Gubler, Mary-Lou,Wertheimer, Stanley J.

, p. 3607 - 3610 (2007/10/03)

The first non-substrate like inhibitors of human cytosolic phosphoenolpyruvate carboxykinase (PEPCK) competitive with GTP are reported. An effort to discover orally active compounds that improve glucose homeostasis in Type 2 diabetics by reversibly inhibi

Di- or trisubstituted xanthines with neuroleptic properties and composition

-

, (2008/06/13)

The invention relates to xanthines corresponding to the formula STR1 and physiologically acceptable salts thereof, in which R1 represents C2 -C4 -alkyl, C3 -C4 -isoalkyl, CH2 -(C2 -C3 -alkenyl) or CH2 -(C3 -isoalkenyl); R3 represents C3 -C5 -alkyl, C3 -C5 -isoalkyl, CH2 -(C2 -C4 -alkenyl) or CH2 -(C3 -C4 -isoalkenyl); R8 represents H, methyl or ethyl; with the proviso that (1) when R8 represents H, R1 is allyl and (2) R1 and R3 cannot both represent butyl or allyl at the same time. The compounds show non-specific or anxiolytic sedative activity.

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