CAS 52218-37-8

5-(acetylamino)naphthalene-1-sulfonyl chloride

Description:

5-(Acetylamino)naphthalene-1-sulfonyl chloride, with the CAS number 52218-37-8, is an organic compound characterized by its sulfonyl chloride functional group attached to a naphthalene ring. This compound features an acetylamino group, which contributes to its reactivity and potential applications in organic synthesis. It is typically a solid at room temperature and may exhibit a crystalline structure. The presence of the sulfonyl chloride group makes it a useful reagent in various chemical reactions, particularly in the synthesis of sulfonamides and other derivatives. It is important to handle this compound with care, as sulfonyl chlorides can be reactive and may release hydrochloric acid upon hydrolysis. Additionally, it may have applications in the development of pharmaceuticals or as an intermediate in the synthesis of more complex organic molecules. Proper safety measures should be observed when working with this compound due to its potential hazards.

Formula: C₁₂H₁₀ClNO₃S

InChI: InChI=1/C12H10ClNO3S/c1-8(15)14-11-6-2-5-10-9(11)4-3-7-12(10)18(13,16)17/h2-7H,1H3,(H,14,15)

SMILES: CC(=Nc1cccc2c1cccc2S(=O)(=O)Cl)O

5-Acetamidonaphthalene-1-sulfonyl chloride

CAS: 52218-37-8

Formula: C₁₂H₁₀ClNO₃S

Purity: 97%

Color and Shape: Solid

Molecular weight: 283.7307

Ref: IN-DA00DF8G

5-Acetamidonaphthalene-1-sulfonyl chloride

CAS: 52218-37-8

5-Acetamidonaphthalene-1-sulfonyl chloride

Purity: 97%

Molecular weight: 283.74g/mol

Ref: 54-OR1058023

5-Acetamidonaphthalene-1-sulfonyl Chloride

Controlled Product

CAS: 52218-37-8

Stability Moisture Sensitive
Applications 5-Acetamidonaphthalene-1-sulfonyl Chloride (cas# 52218-37-8) is a compound useful in organic synthesis.
References Bradbury, R., et al.: J. Med. Chem., 40, 996 (1997),

Formula: C₁₂H₁₀ClNO₃S

Color and Shape: Beige To Yellow

Molecular weight: 283.73

Ref: TR-A158465