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Glycine, N-(phenylthioxomethyl)-, also known as 2-(phenylthiomethyl)glycine or PTMG, is a chemical compound with the molecular formula C9H11NO2S. It is a derivative of glycine, an amino acid, and features a phenylthiomethyl group attached to the nitrogen atom. PTMG is a colorless, crystalline solid that is soluble in water and various organic solvents. Glycine, N-(phenylthioxomethyl)- is primarily used as a monomer in the production of polyether-polyurethane elastomers, which are known for their excellent mechanical properties, flexibility, and resistance to abrasion and chemicals. PTMG is also used in the synthesis of other organic compounds and as a reagent in various chemical reactions.

2584-64-7

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2584-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2584-64-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2584-64:
(6*2)+(5*5)+(4*8)+(3*4)+(2*6)+(1*4)=97
97 % 10 = 7
So 2584-64-7 is a valid CAS Registry Number.

2584-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(benzenecarbonothioylamino)acetic acid

1.2 Other means of identification

Product number -
Other names Glycine,N-(phenylthioxomethyl)

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:2584-64-7 SDS

2584-64-7Relevant academic research and scientific papers

Sonogashira coupling of functionalized trifloyl oxazoles and thiazoles with terminal alkynes: Synthesis of disubstituted heterocycles

Langille, Neil F.,Dakin, Les A.,Panek, James S.

, p. 2485 - 2488 (2007/10/03)

(Matrix presented) This paper describes Sonogashira cross-coupling of functionalized 2-, 4-, and 5-trifloyl oxazoles and thiazoles with terminal alkynes. This methodology has been extended to 2,4-ditrifloylthiazoles, which results in regioselective cross-coupling at the C2-position of the thiazole. The resulting 2-alkynyl-4-trifloylthiazoles are effective electrophiles in a second palladium(0)-mediated cross-coupling reaction.

A total synthesis and structural aspects of racemic 8-oxygenated tetracyclines

Glatz,Helmchen,Muxfeldt,et al.

, p. 2171 - 2181 (2007/10/04)

A stereoselective total synthesis of the first 8-oxygenated tetracycline derivatives 43 and 4 is described. Key steps for the construction of the tetracycline skeleton are the condensation of the tetralone aldehyde 24 with the thiazolone 32 followed by co

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