89284-67-3

Basic information

• Product Name: Benzene, 1-azido-4-chloro-2-nitro-
• CAS NO: 89284-67-3
• Molecular Formula: C6H3ClN4O2
• Molecular Weight: 198.568
• Mol File: 89284-67-3.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzene, 1-azido-4-chloro-2-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-azido-4-chloro-2-nitro-(89284-67-3)
• EPA Substance Registry System: Benzene, 1-azido-4-chloro-2-nitro-(89284-67-3)

Safety Data

• Hazardous Substances Data: 89284-67-3(Hazardous Substances Data)

Upstream product

• 345-18-6 2-fluoro-5-chloronitrobenzene 
• 106-47-8 4-chloro-aniline 
• 881-51-6 N-(4-chloro-2-nitrophenyl)-acetamide 
• 89-63-4 4-Chloro-2-nitroaniline 

Downstream Products

• 145326-34-7 (4-Chloro-2-nitro-phenyl)-[1-morpholin-4-yl-prop-(E)-ylidene]-amine 
• 149179-58-8 1-(4-Chloro-2-nitrophenyl)-4,5-dihydro-4-methyl-5-morpholino-1,2,3-triazole 
• 206976-36-5 1-(4-Chloro-2-nitro-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester 
• 89-63-4 4-Chloro-2-nitroaniline 
• 39060-31-6 6-chlorobenzo[c][1,2,5]oxadiazole 1-oxide 
• 210989-45-0 1-(4-Chloro-2-nitro-phenyl)-5-ethoxycarbonylmethyl-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester 
• 521959-54-6 1-(2-nitro-4-chloro-phenyl)-4-carboxamido-5-amino-1H-1,2,3-triazole 
• 690638-45-0 1-(2'-nitro-4'-chlorophenyl)-5-(4'-nitrophenyl)-1H-1,2,3-triazole-4-carboxylic acid 
• 690638-33-6 1-(4-chloro-2-nitro-phenyl)-5-(4-nitro-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester 

Relevant articles and documents

Synthesis of New Thieno[2,3-d]pyrimidines Containing a 1,2,3-Triazole Ring and Their Therapeutic Response in NCI-60 Cell Line Panel

Abstract: A series of new tetrahydro[1]benzothieno[2,3-d]pyrimidines containing a 1,2,3-triazole fragment linkedthrough an oxymethylene spacer have been synthesized by click reaction of4-(prop-2-yn-1-yloxy)-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidines with various aryl and alkyl azides inthe presence of copper sulfate and sodium ascorbate as a catalyst. Thestructures of the synthesized compounds were characterized by variousspectroscopic techniques (1H and13C NMR, FT-IR, and mass spectrometry), and theirin vitro anticancer activity against NCI-60 human tumor cell lines wasevaluated. Among the compounds tested, N-(pyridine-3-yl)-acetamide derivative exhibited significantactivity against several cancer cell lines, including SF-539 (CNS cancer),HCT-116 (colon cancer), OVCAR-8 (ovarian cancer), PC-3 (prostate cancer), andCCRF-CEM (leukemia).

Click Variations on the Synthesis of 2-Nitrophenyl-4-aryl-1,2,3-triazoles without Isolation of 2-Nitrophenyl Azides

We report a series of efficient procedures to prepare 2-nitrophenyl-4-aryl-1,2,3-triazoles avoiding the isolation of potentially hazardous 2-nitrophenyl azides. An organocatalyzed azide-enolate variant allows efficient access to the target compounds while

Synthesis and characterization of newly fused 1,2-dihydropyrido[3,4-b], bridged oxadiazol-2-yl, 4-substituted-benzylidene hydrazide and arylidene 6-chloroquinoxaline 1,4-dioxides

Some simple reactions using commercially available chemicals were used in the preparation of new biologically remarkable quinoxaline 1,4-dioxide derivatives. Several steps performed on 4-chloro-2-nitroaniline resulted in a quinoxaline 1,4-dioxide derivati