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86872-78-8

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86872-78-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86872-78-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,7 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86872-78:
(7*8)+(6*6)+(5*8)+(4*7)+(3*2)+(2*7)+(1*8)=188
188 % 10 = 8
So 86872-78-8 is a valid CAS Registry Number.

86872-78-8SDS

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 1,3-Diethyl-5-[4-(dimethylamino)benzylidene]-2-thiobarbituric acid

1.2 Other means of identification

Product number -
Other names 1,3-Diaethyl-5-(4-dimethylamino-benzyliden)-2-thio-barbitursaeure

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:86872-78-8 SDS

86872-78-8Downstream Products

86872-78-8Relevant articles and documents

Reactions of l, 3-diethyl-2-thiobarbituric acid with aldehydes: Formation of arylbis(l, 3-diethyl-2-thiobarbitur-5-yl)methanesf and crystallographic evidence for ground state polarisation in l, 3-diethyl-5-[4-(dimethylamino)benzylidene]-2-thiobarbituric a

Adamson, Jason,Coe, Benjamin J.,Grassam, Helen L.,Jeffery, John C.,Coles, Simon J.,Hursthouse, Michael B.

, p. 2483 - 2488 (1999)

The reactions of 1, 3-diethyl-2-thiobarbituric acid (detba) in ethanol at room temperature with 4-(dimethylamino)benzaldehyde (dmabza) or cinnamaldehyde afford the Knoevenagel products 3 and 4, respectively. Under identical conditions, pyridine-4-carbalde

Acetylcholinesterase and butyrylcholinesterase inhibitory activities of 5-arylidene-N, N-diethylthiobarbiturates

Khan, Momin,Rehman, Munir Ur,Qadir, Naveed,Ashraf, Muhammad,Ismail, Tayaba,Ismail, Muhammad,Kanwal,Salar, Uzma,Khan, Khalid Mohammed,Perveen, Shahnaz

, p. 134 - 140 (2020/02/13)

5-Arylidene-N,N-diethylthiobarbiturates 1-25 were evaluated for their potential against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes and displayed varying degree of inhibition. Based on the IC50 values, compound 6 (ICsu

Synthesis, molecular modeling and biological evaluation of 5-arylidene- N,N-diethylthiobarbiturates as potential α-glucosidase Inhibitors

Ashraf, Muhammad,Hameed, Abdul,Hussain, Zahid,Khan, Abbas,Khan, Iltaf,Khan, Khalid M.,Khan, Momin,Khan, Sehrish,Perveen, Shahnaz,Rahman, Jameel,Shams, Sulaiman,Ul Mulk, Amir,Ur Rahman, Anis,Wadood, Abdul,Zaman, Khair

, p. 175 - 185 (2019/07/12)

Background: Barbituric acid derivatives are a versatile group of compounds which are identified as potential pharmacophores for the treatment of anxiety, epilepsy and other psychiatric disorders. They are also used as anesthetics and have sound effects on

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