172468-38-1

Basic information

• Product Name: 4-Azidobutanol 1-Acetate
• Synonyms: 4-Azidobutanol 1-Acetate
• CAS NO: 172468-38-1
• Molecular Formula: C₆H₁₁N₃O₂
• Molecular Weight: 157.17044
• Product Categories: Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 172468-38-1.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• Storage Temp.: Refrigerator
• Solubility: Acetone, Chloroform, Dichloromethane, Toluene
• CAS DataBase Reference: 4-Azidobutanol 1-Acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Azidobutanol 1-Acetate(172468-38-1)
• EPA Substance Registry System: 4-Azidobutanol 1-Acetate(172468-38-1)

Safety Data

• Hazardous Substances Data: 172468-38-1(Hazardous Substances Data)

Usage

Description

4-Azidobutanol 1-Acetate is an organic compound with the chemical formula C6H11N3O4. It is a colorless oil and is primarily used in the synthesis of various pharmaceutical compounds.

Uses

Used in Pharmaceutical Industry:
4-Azidobutanol 1-Acetate is used as an intermediate in the synthesis of Acyclovir and HBG analogs for their development and production. Acyclovir is an antiviral medication used to treat infections caused by herpes viruses, while HBG analogs have potential applications in the treatment of various diseases.

Upstream product

• 4224-62-8 6-chlorohexanoic acid 
• 4753-59-7 4-Bromobutyl acetate 
• 6962-92-1 4-Chlorobutyl acetate 

Downstream Products

• 389131-94-6 toluenesulfonic acid 3-azidobutyl ester 
• 402823-42-1 1-[1-(4-acetoxybutyl)-1,2,3-triazol-5-ylmethyl]-4-benzylthio-1H-pyrazolo[3,4-d]pyrimidine 

Relevant articles and documents

SYNTHESIS OF ALKYL β-GLYCOSIDES OF 6-(N-ACETYLMURAMOYL-L-ALANYL-D-ISOGLUTAMINYLAMINO)HEXANOIC ACID AND ITS 4-AMINOBUTYL ESTER.

The synthesis has been effected of alkyl β-glycosides containing spacers with amino and carboxy groups at the end.As "prespacers" we used benzyl and 4-azidobutyl esters of 6-(L-alanyl-D-isoglutaminylamino)hexanoic acid.The use of the butyl and hexadecyl β

Solid-phase supports and uses thereof

The present disclosure relates to solid-phase azide supports, methods for making solid-state azide supports, and methods for capturing alkynes using the same. The present disclosure also relates to kits for solid-phase azide supports.

Synthesis of acyclovir and HBG analogues having nicotinonitrile and its 2-methyloxy 1,2,3-triazole

Reaction of pyridin-2(1H)-one 1 with 4-bromobutylacetate (2), (2-acetoxyethoxy)methyl bromide (3) gave the corresponding nicotinonitrile O-acyclonucleosides, 4 and 5, respectively. Deacetylation of 4 and 5 gave the corresponding deprotected acyclonucleosi

Synthesis and biological evaluation of some 4-substituted 1-[1-(4-hydroxybutyl)-1,2,3-triazol-(4 & 5)-ylmethyl]-1H-pyrazolo [3,4-d]pyrimidines

The synthesis of 1-[1-(4-hydroxybutyl)-1,2,3-triazol-(4 and 5)-ylmethyl]-1H-pyrazolo[3,4-d] pyrimidines 11a,b, 12a,b and 13-17 as carboacyclic nucleosides is described. The compounds 8a,b were condensed, separately, with compound 7 via 1,3-dipolar cycload