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1,8-NAPHTHOSULTAM

  • CAS：603-72-5
  • purity：99%
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1.What is the 1,8-NAPHTHOSULTAM ?

1,8-naphthyl amine sulphonic acid potassium salt
16619-06-0

1,8-naphthyl amine sulphonic acid potassium salt

1,8-naphthosultam
603-72-5

1,8-naphthosultam

Conditions
Conditions Yield
With trichlorophosphate; at 130 ℃; for 3h;
70%
With trichlorophosphate; at 130 ℃; for 3h;
N-[(Z)-2-(4-methylphenylsulfonyl)ethenyl]-1,8-naphthosultam

N-[(Z)-2-(4-methylphenylsulfonyl)ethenyl]-1,8-naphthosultam

1,8-naphthosultam
603-72-5

1,8-naphthosultam

Conditions
Conditions Yield
With sodium hydride; 1-dodecylthiol; In tetrahydrofuran; at 20 ℃; for 2h; Inert atmosphere;
95%

2.What is the CAS number for 1,8-NAPHTHOSULTAM ?

The CAS number of 1,8-NAPHTHOSULTAM is 603-72-5.

More information of 1,8-NAPHTHOSULTAM 603-72-5 are:

CAS?Number

603-72-5

Density

1.492g/cm3

Melting Point

173-175 °C(lit.)

Boiling Point

442.2°C at 760 mmHg

Flash Point

221.2°C

Vapor Pressure

5.11E-08mmHg at 25°C

Refractive Index

1.5250 (estimate)

HS CODE

2934991000

PSA

54.55000

LogP

3.17280

3.What are another words for 1,8-NAPHTHOSULTAM ?

Synonyms?for?1,8-NAPHTHOSULTAM 603-72-5:1,8-Naphthosultam(6CI,7CI); 2H-Naphtho[1,8-cd]isothiazole 1,1-dioxide

4.What is the molecular formula of 1,8-NAPHTHOSULTAM?

The chemical formula of ?1,8-NAPHTHOSULTAM is?C10H7 N O2 S which containing 10 Carbon atoms,7 Hydrogen atoms,1 Nitrogen atoms,2 Oxygen atoms and 1 Sulfur atoms,and the molecular weight of??1,8-NAPHTHOSULTAM?is 205.237.

5.What is 1,8-NAPHTHOSULTAM (603-72-5) used for?

1,8-Naphthosultam is a sultam derivative that undergoes Friedel-Crafts reactions with acyl-, aroyl-, and arylsulfonyl chlorides in the presence of aluminum chloride, leading to 4-acylated products. It also exhibits rearrangement behavior, where N-acylated and N-arylsulfonyl derivatives migrate substituents to the 4-position under aluminum chloride catalysis or thermal conditions. These reactions highlight its reactivity as a substrate for electrophilic aromatic substitution and rearrangement processes.

InChI:InChI=1/C10H7NO2S/c12-14(13)9-6-2-4-7-3-1-5-8(11-14)10(7)9/h1-6,11H

Relevant articles related to 1,8-NAPHTHOSULTAM:

Article

Source

General synthetic approach towards annelated 3a,6-epoxyisoindoles by tandem acylation/IMDAF reaction of furylazaheterocycles. Scope and limitations

Zubkov, Fedor I.,Nikitina, Eugenia V.,Galeev, Timur R.,Zaytsev, Vladimir P.,Khrustalev, Victor N.,Novikov, Roman A.,Orlova, Daria N.,Varlamov, Alexey V.

, p. 1659 - 1690 (2014/02/14)

Design and synthesis of benzo[c,d]indolone-pyrrolobenzodiazepine conjugates as potential anticancer agents

Kamal, Ahmed,Ramakrishna,Lakshma Nayak,Raju,Subba Rao,Viswanath,Vishnuvardhan,Ramakrishna, Sistla,Srinivas

experimental part, p. 789 - 800 (2012/03/27)

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