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144254-93-3

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144254-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144254-93-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,2,5 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 144254-93:
(8*1)+(7*4)+(6*4)+(5*2)+(4*5)+(3*4)+(2*9)+(1*3)=123
123 % 10 = 3
So 144254-93-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O2S.Na/c1-4-3-5(2)12-9-6(4)7(11)8(15-9)10(13)14;/h3H,11H2,1-2H3,(H,13,14);/q;+1/p-1

144254-93-3SDS

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 sodium,3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names sodium 3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carboxylate

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:144254-93-3 SDS

144254-93-3Relevant articles and documents

SOME REACTIONS OF 3-AMINO-2-CARBOETHOXY-4,6-DIMETHYLTHIENOPYRIDINE. SYNTHESIS OF SOME NEW THIENOPYRIDINOPYRIMIDINES

Hassan, Kh. M.,El-Dean, A.M. Kamal,Youssef, M. S. K.,Atta, F. M.,Abbady, M. S.

, p. 283 - 289 (2007/10/02)

Thienopyridine oxazinone (1) has been prepared and explored as a precursor by its reaction with some reagents namely, ammonium acetate, aliphatic amines, aromatic amines, hydrazine hydrate, thiosemicarbazide, and ethyl glycinate to give pyridothienopyrimidines (II-VII).The pyrimidinone compound (II) was converted to the 4-chloro derivative (X) by its reaction with excess POCl3.Interaction of the 4-chlorocompound (X) with some reagents namely, hydrazine hydrate, methyl amine, aniline, sodium thiophenolate, ethyl glycinate, thiosemicarbazide and thiourea, yielded pyridothieno-pyrimidine derivatives (XI-XVII) substituted at 4-position, respectively.

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