91633-32-8

Basic information

• Product Name: Benzene, 1-(1-azidoethyl)-4-chloro-
• CAS NO: 91633-32-8
• Molecular Formula: C8H8ClN3
• Molecular Weight: 181.625
• Mol File: 91633-32-8.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(1-azidoethyl)-4-chloro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(1-azidoethyl)-4-chloro-(91633-32-8)
• EPA Substance Registry System: Benzene, 1-(1-azidoethyl)-4-chloro-(91633-32-8)

Safety Data

• Hazardous Substances Data: 91633-32-8(Hazardous Substances Data)

Upstream product

• 3391-10-4 1-(p-chlorophenyl)ethyl alcohol 
• 99-91-2 para-chloroacetophenone 
• 75230-50-1 p-chloroacetophenone tosylhydrazone 
• 20001-59-6 1-(4-chlorophenyl)-ethyl methyl ether 
• 92916-02-4 (+/-)-3-(p-chlorophenyl)butan-2-one 
• 76-05-1 trifluoroacetic acid 
• 103966-61-6 1-(4-chlorophenyl)ethyl acetate 
• 1073-67-2 4-vinylbenzyl chloride 

Downstream Products

• 99-91-2 para-chloroacetophenone 
• 208118-80-3 1-(4-chlorophenyl)ethenylacetamide 
• 128720-50-3 1-(4-chlorophenyl)ethan-1-imine 

Relevant articles and documents

Design, Synthesis, and Biological Evaluation of Substituted 4,6-Dihydrospiro[[1,2,3]triazolo[4,5- b]pyridine-7,3′-indoline]-2′,5(3 H)-dione Analogues as Potent NS4B Inhibitors for the Treatment of Dengue Virus Infection

A series of substituted 4,6-dihydrospiro[[1,2,3]triazolo[4,5-b]pyridine-7,3′-indoline]-2′,5(3H)-dione analogues were synthesized and evaluated as potent dengue virus inhibitors. Throughout a structure-activity relationship exploration on the amide of the

SUBSTITUTED 4,6-DIHYDROSPIRO[[1,2,3]TRIAZOLO[4,5-B]PYRIDINE-7,3'-INDOLINE]-2',5(3H)-DIONE ANALOGUES

A series of substituted 4,6-dihydrospiro[[1,2,3]triazolo[4,5-b]pyridine-7,3′-indoline]-2′,5(3H)-dione analogues, the use thereof and the preparation thereof.

Highly selective direct azidation of alcohols over a heterogeneous povidone-phosphotungstic solid acid catalyst

A simple protocol for the selective azidation of alcohols is developed using a solid acid hybrid of a povidone and phosphotungstic acid (PVP-PWA) using azidotrimethylsilane as an azide source at room temperature. In a broad substrate scope, various activated as well as unactivated benzylic and diphenyl alcohols were treated smoothly with TMS-N3 to selectively produce only azide products with excellent yields in a very short reaction time of 2 h. FT-IR confirmed the stability of the catalyst with retention of the Keggins structure after the reaction. Recycling experiments demonstrated the reusability of the PVP-PWA (3?:?1) several times without losing its original activity.