625836-85-3

Basic information

• Product Name: 4-benzylmercapto-3-amino-1,8-naphthalic anhydride
• Synonyms: 4-benzylmercapto-3-amino-1,8-naphthalic anhydride
• CAS NO: 625836-85-3
• Molecular Weight: 335.383
• Mol File: 625836-85-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-benzylmercapto-3-amino-1,8-naphthalic anhydride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-benzylmercapto-3-amino-1,8-naphthalic anhydride(625836-85-3)
• EPA Substance Registry System: 4-benzylmercapto-3-amino-1,8-naphthalic anhydride(625836-85-3)

Safety Data

• Hazardous Substances Data: 625836-85-3(Hazardous Substances Data)

Upstream product

• 625836-84-2 4-benzylmercapto-3-nitro-1,8-naphthalic anhydride 
• 100-53-8 phenylmethanethiol 
• 52821-19-9 4-bromo-3-nitro-1,8-naphthalic anhydride 

Relevant articles and documents

SULFUR-CONTAINING NAPHTHOYLIMIDE DERIVATIVES

The invention discloses novel sulfur-containing naphthalimide derivatives, and the preparation and uses thereof. The conjugated plane of naphthalimide derivatives of the invention is enlarged by incorporating 5-or 6-membered heteroaromatic ring and/or introducing S heteroatom, thus increasing the anti-tumor activity of naphthalimide. The compounds of the invention displays significant inhibiting activities to the proliferation of various tumor cells such as human lung cancer, gastric cancer, liver cancer, leucocythemia and the like. The inhibition of cell proliferation is dose-dependent.

Synthesis of thiazo- or thiadiazo- naphthalene carboxamides via mercuric intermediates and their antitumor and DNA photocleavage activities

Two kinds of thiazo- or thiadiazo- naphthalene carboxamides with aminoalkyl side chains at 5- or 6-position modified from naphthalimides were designed, synthesized and quantitatively evaluated as antitumor and DNA photocleaving agents. The compound with a