608132-17-8

Basic information

• Product Name: 4-tertbutyl mercapto-5-tertbutyl mercapto methenyl-1-(2,4-dimethoxy-phenyl)-3-amino-1,5-dihydropyrrolidone
• Synonyms: 4-tertbutyl mercapto-5-tertbutyl mercapto methenyl-1-(2,4-dimethoxy-phenyl)-3-amino-1,5-dihydropyrrolidone
• CAS NO: 608132-17-8
• Molecular Weight: 422.613
• Mol File: 608132-17-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-tertbutyl mercapto-5-tertbutyl mercapto methenyl-1-(2,4-dimethoxy-phenyl)-3-amino-1,5-dihydropyrrolidone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-tertbutyl mercapto-5-tertbutyl mercapto methenyl-1-(2,4-dimethoxy-phenyl)-3-amino-1,5-dihydropyrrolidone(608132-17-8)
• EPA Substance Registry System: 4-tertbutyl mercapto-5-tertbutyl mercapto methenyl-1-(2,4-dimethoxy-phenyl)-3-amino-1,5-dihydropyrrolidone(608132-17-8)

Safety Data

• Hazardous Substances Data: 608132-17-8(Hazardous Substances Data)

Upstream product

• 608132-08-7 4-tertbutyl mercapto-5-tertbutyl mercapto methenyl-1-(2,4-dimethoxy-phenyl)-3-hydroxy-1,5-dihydropyrrolidone 

Downstream Products

• 608132-32-7 4-tertbutyl mercapto-5-tertbutyl mercapto methenyl-1-(2,4-dimethoxy-phenyl)-3-trifluoro acetamido-1,5-dihydropyrrolidone 
• 944799-69-3 N-[4-(2,4-dimethoxyphenyl)-5-oxo-4,5-dihydro[1,2]dithiolo[4,3-b]pyrrol-6-yl]-2,2,2-trifluoroacetamide 
• 1015064-87-5 6-amino-4-(2,4-dimethoxyphenyl)-4H-[1,2]dithioleheterocyclicpentene[4,3-b]-5-pyrrolidonecarboxylic acid ethyl ester 
• 1015064-91-1 [4-(2,4-dimethoxy-phenyl)-5-oxo-4,5-dihydro-[1,2]dithiolo[4,3-b]pyrrol-6-yl]-carbamic acid allyl ester 
• 1015065-18-5 [4-(2,4-dimethoxy-phenyl)-5-oxo-4,5-dihydro-[1,2]dithiolo[4,3-b]pyrrol-6-yl]-carbamic acid 
• 1438425-02-5 C₂₂H₂₀N₂O₅S₂ 
• 1015064-93-3 C₂₁H₁₈N₂O₆S₂ 
• 1438425-05-8 C₁₉H₁₅N₃O₅S₂ 

Relevant articles and documents

Synthesis of substituted 6-amino-4-(2,4-dimethoxyphenyl)-[1,2]dithiolo[ 4,3-b]pyrrol-5-ones and their raising leukocyte count activities

The design and synthesis of a series of substituted 6-amino-4-(2,4- dimethoxyphenyl)-[1,2]dithiolo[4,3-b]pyrrol- 5-ones are described. All the synthesized compounds were evaluated for raising leukocyte count activities in normal mice. Four compounds (8a,

DITHIOLOPYRROLONE COMPOUNDS, THE PREPARATION AND THE USE THEREOF

The invention discloses a dithiolopyrrolone compound represented by formula I or its pharmaceutically acceptable salts, wherein X1, R1, R2, R3, R4 are defined as in the description. The invention also