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169563-66-0

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169563-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169563-66-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,5,6 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 169563-66:
(8*1)+(7*6)+(6*9)+(5*5)+(4*6)+(3*3)+(2*6)+(1*6)=180
180 % 10 = 0
So 169563-66-0 is a valid CAS Registry Number.

169563-66-0SDS

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 N-cyclohexyl-N-(cyclohexylcarbamoyl)-2-(3,7-dimethyl-2,6-dioxopurin-1-yl)acetamide

1.2 Other means of identification

Product number -
Other names 1H-Purine-7-acetamide,2,3,6,7-tetrahydro-N-cyclohexyl-N-((cylohexylamino)carbonyl)-3,7-dimethyl-2,6-dioxo

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:169563-66-0 SDS

169563-66-0Downstream Products

169563-66-0Relevant articles and documents

Synthesis, toxicological, pharmacological, and bronchodilating activity in vitro of some xanthineacetic acid derivatives

Peikov,Danchev,Zlatkov,Ivanov,Belcheva

, p. 615 - 618 (1995)

The possibility of the preparation of some ester derivatives of dimethylxanthines from 1-theobromine- and 7-theophylline acetic acids and 7-(2-hydroxyethyl)-theophylline by DCC/DMAP-mediated esterification under mild conditions was studied. The structures of the compounds synthesized and by products isolated were demonstrated by microanalyses, UV-, IR-, and 1H NMR data. Acute toxicity assessment of the compounds on mice showed that compounds 4, 5, 6, and 7 are less toxic than aminophylline. A pharmacological study of the in vitro broncholytic effect (IC50 and pD2 values) of the derivatives and aminophylline showed that the new compound 4 (1,2,3,6-tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purine-7-acetic acid 2-(1,2,3,6-tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl ester) has a strong bronchodilating effect on serotonine- and acetylcholine-induced spasm in guinea pig trachea. The same compound does not influence barbiturate induced hypnosis and locomotor activity, unlike to the effect of the aminophylline, used as a reference substance.

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