N-Thionylaniline, 95%

Name: N-Thionylaniline, 95% | 1122-83-4
Brand: J&K Chemical
SKU: JK100570_25_G
Price: 59.0 USD
Availability: OutOfStock

Cat. No JK100570_25_G

Vendor: J&K Chemical

Product Information

Product Name

N-Thionylaniline, 95%

Brand Name

J&K

Product Number

100570

CAS

1122-83-4

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

70739

IUPAC Name

(sulfinylamino)benzene

InChI Key

FIOJWGRGPONADF-UHFFFAOYSA-N

SMILES

C1=CC=C(C=C1)N=S=O

Safety Information

Storage Condition

Room temperature

References Data Source From Pubchem

Organocatalytic enantioselective synthesis of S(IV)-stereogenic sulfinamides enabled by an air-stable chiral phosphine

Publication Name: Nature Chemistry

Publication Date: 2026-03-10

DOI: 10.1038/s41557-026-02095-9

Size-tuned PEGylated NIR-II fluorescent probes for high-contrast plant imaging and TMV detection

Publication Name: Journal of Nanobiotechnology

Publication Date: 2025-06-08

DOI: 10.1186/s12951-025-03452-5

Homologation of Heteroatom Electrophiles

Publication Name: Science of Synthesis

Publication Date: 2025

Synthesis and reactivity of [1, 2, 5]thiadiazolo[3,4-b]pyridines and [1, 2, 5]selenadiazolo[3,4-b]pyridines (microreview)

Publication Name: Chemistry of Heterocyclic Compounds

Publication Date: 2024-02

DOI: 10.1007/s10593-024-03290-7

Dynamic stereochemistry at work: Configurational lability of nitrogen and sulfur atoms within a sulfonamide moiety as a cause of forming supramolecular diastereomers in crystals

Publication Name: Structural Chemistry

Publication Date: 2023-12-10

DOI: 10.1007/s11224-023-02260-7

N-Thionylaniline, 95%

Product Information

General Information

Safety Information

References Data Source From Pubchem

Organocatalytic enantioselective synthesis of S(IV)-stereogenic sulfinamides enabled by an air-stable chiral phosphine

Size-tuned PEGylated NIR-II fluorescent probes for high-contrast plant imaging and TMV detection

Homologation of Heteroatom Electrophiles

Synthesis and reactivity of [1, 2, 5]thiadiazolo[3,4-b]pyridines and [1, 2, 5]selenadiazolo[3,4-b]pyridines (microreview)

Dynamic stereochemistry at work: Configurational lability of nitrogen and sulfur atoms within a sulfonamide moiety as a cause of forming supramolecular diastereomers in crystals