2-Methoxy-5,6,6-trimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide

Base Information

• Chemical Name: 2-Methoxy-5,6,6-trimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide
• CAS No.: 36743-52-9
• Molecular Formula: C7H13NO4S
• Molecular Weight: 207.2474
• NSC Number: 174530

Synonyms:36743-52-9;2-Methoxy-5,6,6-trimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide;NSC174530;NSC 174530;2-methoxy-5,6,6-trimethyl-5H-1,4,3-oxathiazine 4,4-dioxide;Methyl 5,6,6-trimethyl-4,4-dioxido-5,6-dihydro-1,4,3-oxathiazin-2-yl ether;NSC-174530;2-methoxy-5,6,6-trimethyl-5H-[1,4,3]oxathiazine 4,4-dioxide

Chemical Property of 2-Methoxy-5,6,6-trimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide

Chemical Property:

• Vapor Pressure: 0.0259mmHg at 25°C
• Boiling Point: 255.6°Cat760mmHg
• Flash Point: 108.4°C
• Density: 1.32g/cm³
• XLogP3: 1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 1
• Exact Mass: 207.05652907
• Heavy Atom Count: 13
• Complexity: 325

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC1C(OC(=NS1(=O)=O)OC)(C)C

Technology Process of 2-Methoxy-5,6,6-trimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide

There total 2 articles about 2-Methoxy-5,6,6-trimethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide 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:

4-Methoxystyrene (637-69-4,24936-44-5) + tetrahydrofuran; compound with sulfonylcarbamic acid methyl ester (36743-45-0) → 2,3-Dihydro-2,2,3-trimethyl-6-methoxy-1,4,5-oxathiazin-4,4-dioxid (36743-52-9)

Guidance literature:

In tetrahydrofuran; at 30 ℃;

DOI:10.1021/ja00767a082

Reference yield:

2-methyl-but-2-ene (513-35-9) + tetrahydrofuran; compound with sulfonylcarbamic acid methyl ester (36743-45-0) → 3,3,4-trimethyl-1,1-dioxo-1λ6-[1,2]thiazetidine-2-carboxylic acid methyl ester (36743-51-8) + 2,3-Dihydro-2,2,3-trimethyl-6-methoxy-1,4,5-oxathiazin-4,4-dioxid (36743-52-9)

Guidance literature:

In acetonitrile; at 30 ℃;

DOI:10.1021/ja00767a082

upstream raw materials:

4-Methoxystyrene

tetrahydrofuran; compound with sulfonylcarbamic acid methyl ester

2-methyl-but-2-ene

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