Methyl 2-phenylthioamidoacetate

Base Information

Chemical Name:Methyl 2-phenylthioamidoacetate
CAS No.:35960-95-3
Molecular Formula:C9H9NO3S
Molecular Weight:211.23766
Hs Code.:2930909090
DSSTox Substance ID:DTXSID70573418
Wikidata:Q82462141
Mol file:35960-95-3.mol

Synonyms:Methyl 2-phenylthioamidoacetate;35960-95-3;methyl (benzothioylamino)acetate;methyl 2-(benzenecarbonothioylamino)acetate;methyl (phenylcarbonothioyl)glycinate;METHYL 2-(PHENYLMETHANETHIOAMIDO)ACETATE;Methyl2-phenylthioamidoacetate;DTXSID70573418;Methyl N-(benzenecarbothioyl)glycinate;A874488;AL-398/40365441

Suppliers and Price of Methyl 2-phenylthioamidoacetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Crysdot
Methyl2-phenylthioamidoacetate 95+%
1g
$ 313.00

Chemenu
methyl(phenylcarbonothioyl)glycinate 95%
1g
$ 296.00

Alichem
Methyl2-phenylthioamidoacetate
1g
$ 400.00

Total 4 raw suppliers

Chemical Property of Methyl 2-phenylthioamidoacetate

Chemical Property:

PSA：77.46000
LogP:1.53600
Storage Temp.:2-8°C
XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:209.05104977
Heavy Atom Count:14
Complexity:212

Purity/Quality:

97% ^*data from raw suppliers

Methyl2-phenylthioamidoacetate 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)CNC(=S)C1=CC=CC=C1

Technology Process of Methyl 2-phenylthioamidoacetate

There total 6 articles about Methyl 2-phenylthioamidoacetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 87.0%

: 98-91-9
thiobenzoic acid

: 1816-92-8
Methyl azidoacetate

: 1205-08-9
methyl hippurate

: 35960-95-3
methyl N-(thiobenzoyl)glycinate

Guidance literature:: With triphenylphosphine; In neat (no solvent); at 180 ℃; for 0.25h; chemoselective reaction; Microwave irradiation;
DOI:10.1080/00397911.2011.606043

Reference yield: 83.0%

: 1816-92-8
Methyl azidoacetate

: 2168-78-7
methyl dithiobenzoate

: 35960-95-3
methyl N-(thiobenzoyl)glycinate

: 38648-75-8
methyl N-[α-(methylsulfanyl)benzylidene]glycinate

Guidance literature:: at 110 - 150 ℃; for 10h;

Reference yield:

: phenylmagnesium bromide

: 35960-95-3
methyl N-(thiobenzoyl)glycinate

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether / Behandeln des Reaktionsprodukts mit wss. Natrium-chloracetat

2: aqueous NaOH

With sodium hydroxide; diethyl ether;
DOI:10.1007/BF03019812