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2-methyl-2,3,6,7,8,9-hexahydro-5H-[1]benzothieno[2,3-d][1,3]thiazolo[3,2-a]pyrimidin-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52881-31-9

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52881-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52881-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,8 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52881-31:
(7*5)+(6*2)+(5*8)+(4*8)+(3*1)+(2*3)+(1*1)=129
129 % 10 = 9
So 52881-31-9 is a valid CAS Registry Number.

52881-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-2,3,6,7,8,9-hexahydro-benzo[4,5]thieno[2,3-d]thiazolo[3,2-a]pyrimidin-5-one

1.2 Other means of identification

Product number -
Other names 2-methyl-4,6,7,8,9-pentahydro-2H,3H-benzo[b]thiopheno[2,3-d]1,3-thiazolidino[3,2-a]pyrimidin-5-one

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:52881-31-9 SDS

52881-31-9Downstream Products

52881-31-9Relevant academic research and scientific papers

Synthesis of 3 substituted thieno[2,3 d]pyrimidin 4(3H) one 2 mercaptoacetic acids and their ethyl esters for pharmacological screening

Devani,Shishoo,Pathak,Parikh,Shah,Padhya

, p. 660 - 664 (2007/10/08)

3 Substituted thieno[2,3 d]pyrimidin 4(3H) one 2 mercaptoacetic acids and their ethyl esters were synthesized from 2 mercaptothieno[2,3 d]pyrimidin 4 (3H) ones, which were obtained by cyclization of thienylthioureas in acidic medium. Analgesic, anti inflammatory, and anticonvulsant activities were found in some of these compounds. Significant antimicrobial activity was exhibited by thienylthioureas.

Synthesis of 2-methylene-2,3-dihydro-and 2-methyl-5H-thiazolo[3.2-a]thieno[2.3-d]pyrimidines

Sauter,Deinhammer,Danksagmueller

, p. 863 - 868 (2007/10/05)

The title substances and their [1]benzothieno analogues were synthesized by reaction of 3-allyl-2-mercapto-([1]benzo)thieno-[2.3-d]pyrimidine-4(3 H)-ones with Br2 to 2-bromomethyl-2.3-dihydro-thiazolo[3.2-a]([1]benzo-)thieno[2.3-d]pyrimidine-5-ones, which on treatment with morpholine did not give the corresponding morpholine derivatives but elimination to the exocyclic double bond. These 2-methylene-2.3-dihydro-products were isomerized by H2SO4 to the corresponding 2-methyl compounds.

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