27032-10-6

Basic information

• Product Name: p-Chlorobenzyl azide solution
• Synonyms: 1-(Azidomethyl)-4-chlorobenzene solution;p-Chlorobenzyl azide solution;1-(Azidomethyl)-4-chlorobenzene solution ~0.5 M in dichloromethane, >=97.0% (GC)
• CAS NO: 27032-10-6
• Molecular Formula: C₇H₆ClN₃
• Molecular Weight: 167.6
• Mol File: 27032-10-6.mol
• Article Data: 107

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• BRN: 2441922
• CAS DataBase Reference: p-Chlorobenzyl azide solution(CAS DataBase Reference)
• NIST Chemistry Reference: p-Chlorobenzyl azide solution(27032-10-6)
• EPA Substance Registry System: p-Chlorobenzyl azide solution(27032-10-6)

Safety Data

• Hazard Codes: Xn
• Statements: 40-48/20/21/22
• Safety Statements: 36/37
• RIDADR: UN 1593 6.1 / PGIII
• WGK Germany: 3
• Hazardous Substances Data: 27032-10-6(Hazardous Substances Data)

Upstream product

• 873-76-7 para-Chlorobenzyl alcohol 
• 78358-09-5 40chlorobenzyl methanesulfonate 
• 104-83-6 1-Chloro-4-(chloromethyl)benzene 
• 4450-67-3 4-chlorobenzyl 4-methylbenzenesulfonate 
• 5651-83-2 3-methoxy-4-(prop-2-ynyloxy)benzaldehyde 
• 622-95-7 4-chlorobenzyl bromide 
• 74-11-3 para-chlorobenzoic acid 
• 106-43-4 para-chlorotoluene 
• 108-90-7 chlorobenzene 
• 104-86-9 4-chlorobenzylamine 
• 104-88-1 4-chlorobenzaldehyde 
• 76053-06-0 1-(p-Chlorbenzyl)-3-cyanpyridiniumchlorid 

Downstream Products

• 141072-00-6 di-tert-butyl 1-(4-chlorobenzyl)-1H-1,2,3-triazole-4,5-dicarboxylate 
• 141072-13-1 methyl 1-(4-chlorobenzyl)-1H-1,2,3-triazole-4-carboxylate 
• 132269-38-6 5-Amino-1-(4-chloro-benzyl)-1H-[1,2,3]triazole-4-carboxylic acid amide 
• 104-86-9 4-chlorobenzylamine 
• 932-96-7 N-methyl(p-chloroaniline) 
• 42365-43-5 (4-chlorophenyl)methanamine hydrochloride 
• 126800-07-5 1‐(4‐chlorobenzyl)‐4‐phenyl‐1H‐1,2,3‐triazole 
• 623-03-0 4-Cyanochlorobenzene 
• 1253801-31-8 4-amino-N-((1-(4-chlorobenzyl)-1H-1,2,3-triazol-4-yl)methyl)benzenesulfonamide 
• 1245773-30-1 (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(1-(4-chlorobenzyl)-1H-1,2,3-triazol-4-yl)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate 
• 1270170-26-7 C₁₇H₁₂ClN₃ 
• 133455-49-9 7-chloro-quinoline-3-carboxylic acid ethyl ester 
• 352521-48-3 5-chloroquinoline-3-carboxylic acid ethyl ester 
• 375854-57-2 6-chloroquinoline-3-carboxylic acid ethyl ester 

Relevant articles and documents

Anti-Lung Cancer Activities of 1,2,3-Triazole Curcumin Derivatives via Regulation of the MAPK/NF-κB/STAT3 Signaling Pathways

In this study, a series of curcumin derivatives containing 1,2,3-triazole were designed and synthesized, and their inhibitory activities against the proliferation of lung cancer cells were studied. Compound 5 k (3,4-dichlorobenzyltriazole methyl curcumin)

TDP-43 Modulation by Tau-Tubulin Kinase 1 Inhibitors: A New Avenue for Future Amyotrophic Lateral Sclerosis Therapy

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease without any effective treatment. Protein TDP-43 is a pathological hallmark of ALS in both sporadic and familiar patients. Post-translational modifications of TDP-43 promote its aggre

Synthesis, Docking, and Biological activities of novel Metacetamol embedded [1,2,3]-triazole derivatives

ERα controls the breast tissue development and progression of breast cancer. In our search for novel compounds to target Estrogen Receptor Alpha Ligand-Binding Domain, we identified “N-(3-((1H-1,2,3-triazol-4-yl)methoxy)phenyl)acetamide” derivatives as lead compounds. The Docking studies indicated good docking score for Metacetamol derivatives when docked into the 1XP6. A series of metacetamol derivatives have been synthesized, characterized and evaluated for cytotoxicity, anti bacterial and anti oxidant activities. Among the tested twelve hybrid compounds, “7a, 7g, 7h and 7i” derivatives showed promising cytotoxicity with IC50 value of 50 value of 30 μM, whereas Compounds “7a, 7b, 7c, 7d, 7g, 7j, 7k and 7l” showed moderate anti bacterial activity with the MIC value of 300 μM.