3-[(2-Methylphenyl)sulfonyl]alanine

Base Information

Chemical Name:3-[(2-Methylphenyl)sulfonyl]alanine
CAS No.:103095-43-8
Molecular Formula:C₁₀H₁₃NO₄S
Molecular Weight:243.284
Hs Code.:
NSC Number:19951
DSSTox Substance ID:DTXSID401294646

Synonyms:SCHEMBL7874019;DTXSID401294646;NSC19951;3-[(2-methylphenyl)sulfonyl]alanine;NSC-19951;AKOS014780427;103095-43-8

Suppliers and Price of 3-[(2-Methylphenyl)sulfonyl]alanine

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 3-[(2-Methylphenyl)sulfonyl]alanine

Chemical Property:

XLogP3:-2.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:243.05652907
Heavy Atom Count:16
Complexity:346

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=CC=C1S(=O)(=O)CC(C(=O)O)N

Technology Process of 3-[(2-Methylphenyl)sulfonyl]alanine

There total 2 articles about 3-[(2-Methylphenyl)sulfonyl]alanine 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:

: 5437-55-8
S-o-tolyl-DL-cysteine

: 103095-43-8
2-amino-3-(toluene-2-sulfonyl)-propionic acid

Guidance literature:: With dihydrogen peroxide; acetic acid;
DOI:10.1021/jo01103a004

Reference yield:

: 137-06-4
2-thiocresol

: 103095-43-8
2-amino-3-(toluene-2-sulfonyl)-propionic acid

Guidance literature:: Multi-step reaction with 3 steps

1: dioxane; piperidine

2: aqueous H₂SO₄

3: aqueous H₂O₂; acetic acid

With piperidine; 1,4-dioxane; sulfuric acid; dihydrogen peroxide; acetic acid;
DOI:10.1021/jo01103a004