Sulfide, nitroso trityl

Base Information

• Chemical Name: Sulfide, nitroso trityl
• CAS No.: 6316-86-5
• Molecular Formula: C19H15NOS
• Molecular Weight: 305.4
• NSC Number: 22519
• UNII: EDT6XKN756
• DSSTox Substance ID: DTXSID80212503
• Nikkaji Number: J90.668I
• Wikidata: Q83087646
• Mol file: 6316-86-5.mol

Synonyms:Sulfide, nitroso trityl;Trityl thionitrite;S-Trityl thionitrite;Nitroso trityl sulfide;6316-86-5;Thionitrous acid (HNOS), S-(triphenylmethyl) ester;NSC 22519;[nitrososulfanyl(diphenyl)methyl]benzene;BRN 2133826;EDT6XKN756;C19H15NOS;NSC-22519;Trityl thionitrite, Ph3CSNO;Tritylnitroso sulfide;trityl-s-nitrosothiol;Ph3CSNO;UNII-EDT6XKN756;Nitroso-triphenylmethanethiol;S-Nitroso-triphenylmethanethiol;SCHEMBL4031910;DTXSID80212503;C19-H15-N-O-S;NSC22519;THIONITROUS ACID, S-TRITYL ESTER;METHANETHIOL, TRIPHENYL-, NITRITE;LS-147937;Acetamide, 2-(diethylamino)-N-(2,3-dihydro-2-phenyl-1H-inden-1-yl)-, monohydrochloride

Chemical Property of Sulfide, nitroso trityl

Chemical Property:

• Melting Point: 99.2 °C (decomp)
• Boiling Point: 426.6°Cat760mmHg
• Flash Point: 211.8°C
• PSA: 54.73000
• Density: 1.11g/cm³
• LogP: 5.39310
• XLogP3: 4.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 305.08743528
• Heavy Atom Count: 22
• Complexity: 296

Purity/Quality:

99% ^*data from raw suppliers

NITROSO TRITYL SULFIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)SN=O

Technology Process of Sulfide, nitroso trityl

There total 9 articles about Sulfide, nitroso trityl 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: 75.0%

triphenylmethanethiol (3695-77-0) → trityl thionitrite (6316-86-5)

Guidance literature:

triphenylmethanethiol; With isopentyl nitrite; In dichloromethane; at 20 ℃; Darkness;

With methanol; In dichloromethane; at -25 ℃; for 2h; Darkness;

DOI:10.1021/ja8054996

Reference yield:

2-nitro-2-nitrosopropane (5275-46-7) + triphenylmethanethiol (3695-77-0) → 2-nitropropane (79-46-9) + trityl thionitrite (6316-86-5)

Guidance literature:

In acetonitrile; at 25 ℃; Equilibrium constant;

DOI:10.1021/jo900732b

Reference yield:

iron(III) chloride + nitrogen(II) oxide (10102-43-9) + tetrabutylammonium salt of triphenylmethanethiol → trityl thionitrite (6316-86-5) + tetrabutylammonium[Cl3FeNO]

Guidance literature:

In tetrahydrofuran-d8; acetonitrile; at -78 ℃; for 2h; Inert atmosphere;

DOI:10.1021/acs.inorgchem.1c00203

upstream raw materials:

ethyl nitrite

triphenylmethanethiol

dinitrogen tetraoxide

sulfuric acid

Downstream raw materials:

ditrityl disulfide

C₁₉H₁₅S

pyridyltriphenylmethyl disulfide

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