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2-MORPHOLIN-4-YL-4-PHENYL-THIAZOLE-5-CARBALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129880-85-9

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129880-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129880-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,8,8 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 129880-85:
(8*1)+(7*2)+(6*9)+(5*8)+(4*8)+(3*0)+(2*8)+(1*5)=169
169 % 10 = 9
So 129880-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H14N2O2S/c17-10-12-13(11-4-2-1-3-5-11)15-14(19-12)16-6-8-18-9-7-16/h1-5,10H,6-9H2

129880-85-9SDS

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-morpholin-4-yl-4-phenyl-1,3-thiazole-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-Thiazolecarboxaldehyde,2-(4-morpholinyl)-4-phenyl

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:129880-85-9 SDS

129880-85-9Downstream Products

129880-85-9Relevant academic research and scientific papers

Synthesis and exploration of 2-morpholino-4-phenylthiazol-5-yl acrylamide derivatives for their effects against carbonic anhydrase I, II, IX and XII isoforms as a non-sulfonamide class of inhibitors

Swain, Baijayantimala,Singh Digwal, Chander,Angeli, Andrea,Alvala, Mallika,Singh, Priti,Supuran, Claudiu T.,Arifuddin, Mohammed

, (2019/09/12)

Novel series of 2-morpholino-4-phenylthiazol-5-yl acrylamide derivatives (8a–s) have been synthesized and explored as a non-sulfonamide class of carbonic anhydrase (CA, EC 4.2.1.1) inhibitors. The newly synthesized molecules were evaluated for their CA in

An Easy General Synthesis of 2-(N,N-Dialkylamino)thiazol-5-yl Aldehydes and Ketones

Sawhney, Indu,Wilson, John R. H.

, p. 329 - 331 (2007/10/02)

Reaction between 2-chloro-5-thiazolyl-lithium and N,N-dialkylformamides or amides gave 2-N,N-dialkylaminothiazol-5-yl aldehydes or ketones on quenching with water.Quenching with acid gave 2-chlorothiazole-5-yl aldehydes or ketones, from which chloride was easily displaced by free amines.

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