130239-34-8

Basic information

• Product Name: 1,3-Butanediol, 4-aMino-
• Synonyms: 1,3-Butanediol, 4-aMino-
• CAS NO: 130239-34-8
• Molecular Formula: C₄H₁₁NO₂
• Molecular Weight: 105.13564
• Mol File: 130239-34-8.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3-Butanediol, 4-aMino-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Butanediol, 4-aMino-(130239-34-8)
• EPA Substance Registry System: 1,3-Butanediol, 4-aMino-(130239-34-8)

Safety Data

• Hazardous Substances Data: 130239-34-8(Hazardous Substances Data)

Upstream product

• 78879-85-3 N-(2,4-dihydroxy-butyl)-phthalimide 
• 79416-52-7 (-)-2-(2-Hydroxyethyl)clavam 
• 157423-40-0 (S)-1-azido-2,4-O-benzylidenebutane 
• 637343-50-1 4-dibenzylamino-1, 3-(S) butanediol 
• 7013-05-0 (S)-4-amino-3-hydroxybutanoic acid 

Downstream Products

• 1092457-56-1 C₁₈H₁₈F₃IN₄O₄ 
• 157423-38-6 (S)-<1-(benzyloxycarbonyl)amino>-butan-2,4-diol 
• 1092457-57-2 C₁₈H₁₈F₃IN₄O₄ 

Relevant articles and documents

Hydrolysis of N-Substituted Phthalimides Using Anion Exchange Resins. Synthesis of Hydroxy-Substituted Aliphatic Primary Amines (Amino Alcohols)

N-Substituted phthalimides were successfully hydrolyzed to the corresponding hydroxy-substituted aliphatic primary amines (amino alcohols) using anion exchange resins.This method has been proved to be extremely useful for water soluble products, which are

EIN NEUES ANTIFUNGISCHES β-LACTAM-ANTIBIOTICUM DER CLAVAM-REIHE

The novel β-lactam-antibiotic (-)-2-(2-hydroxyethyl)clavam (1) originates from cultures of Streptomyces antibioticus.The structure is shown by spectroscopic and degradative methods.

PROCESS FOR THE PREPARATION OF OXAZOLIDINONES AND METHOD OF USE THEREOF

A process for preparing N-(substituted)-C-- (substituted methyl)-oxazolidinones, C-(substituted methyl)-oxazolidinones, and N-(substituted)-C-- (substituted ethyl)-oxazolidinones, preferably chiral, from optically active C-(protected oxymethyl)- oxazolidi

Absolute configuration of C(1)-C(5) fragment of AAL-toxin: Conformationally rigid acyclic aminotriol moiety

Degradation of AAL-toxin 1 a host-specific phytotoxin and synthesis of model aminotriol 7a-7d allowed us to determine the absolute configuration of C(1)-C(5) fragment as 2S, 4S and 5R. Unusually rigid conformation of this acyclic fragment was also discussed.