(3S)-2,2-Dimethyl-1,4-thiazinane-3-carboxylic acid

Base Information

Chemical Name:(3S)-2,2-Dimethyl-1,4-thiazinane-3-carboxylic acid
CAS No.:84915-43-5
Molecular Formula:C₇H₁₃NO₂S
Molecular Weight:175.252
Hs Code.:
DSSTox Substance ID:DTXSID30905014
Wikidata:Q81988352
Mol file:84915-43-5.mol

Synonyms:84915-43-5;(3S)-2,2-DIMETHYL-1,4-THIAZINANE-3-CARBOXYLIC ACID;(S)-2,2-Dimethylthiomorpholine-3-carboxylic acid;(3S)-2,2-DIMETHYLTHIOMORPHOLINE-3-CARBOXYLIC ACID;SCHEMBL1770440;DTXSID30905014;PPNGSCRYZMXTEK-YFKPBYRVSA-N;EN300-1168679;(3S)-2,2-dimethyl-3-thiomorpholine carboxylic acid;(S)-2,2-dimethyl-thiomorpholine-3-carboxylic acid;(3 S)-2,2-dimethyl-3-thiomorpholine carboxylic acid

Suppliers and Price of (3S)-2,2-Dimethyl-1,4-thiazinane-3-carboxylic acid

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

Total 5 raw suppliers

Chemical Property of (3S)-2,2-Dimethyl-1,4-thiazinane-3-carboxylic acid

Chemical Property:

XLogP3:-1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:175.06669983
Heavy Atom Count:11
Complexity:170

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1(C(NCCS1)C(=O)O)C
Isomeric SMILES:CC1([C@@H](NCCS1)C(=O)O)C

Technology Process of (3S)-2,2-Dimethyl-1,4-thiazinane-3-carboxylic acid

There total 7 articles about (3S)-2,2-Dimethyl-1,4-thiazinane-3-carboxylic acid 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:

: 1113-41-3
L-penicillamine

: 107-06-2,52399-93-6
1,2-dichloro-ethane

: 774243-35-5,84915-43-5
3(R)-2,2-dimethyl-tetrahydro-2H-1,4-thiazine-3-carboxylic acid

Guidance literature:: With chloro-trimethyl-silane; 1,8-diazabicyclo[5.4.0]undec-7-ene; In DMF (N,N-dimethyl-formamide); at 0 - 25 ℃; for 20h;

Reference yield:

: 79-37-8
oxalyl dichloride

: 1113-41-3
L-penicillamine

: 774243-35-5,84915-43-5
3(R)-2,2-dimethyl-tetrahydro-2H-1,4-thiazine-3-carboxylic acid

Guidance literature:: oxalyl dichloride; L-penicillamine; With chloro-trimethyl-silane; 1,8-diazabicyclo[5.4.0]undec-7-ene; In DMF (N,N-dimethyl-formamide); at 20 ℃;

With methanol; In DMF (N,N-dimethyl-formamide); for 1h;

Reference yield:

: C₁₃H₂₉NO₂SSi

: 774243-35-5,84915-43-5
3(R)-2,2-dimethyl-tetrahydro-2H-1,4-thiazine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / Inert atmosphere

With tetrabutyl ammonium fluoride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; N,N-dimethyl-formamide;