114809-62-0

Basic information

• Product Name: O-[3-(benzyloxy)propyl]hydroxylamine
• CAS NO: 114809-62-0
• Molecular Formula: C₁₀H₁₅NO₂
• Molecular Weight: 181.2316
• Mol File: 114809-62-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 307.5°C at 760 mmHg
• Flash Point: 149.7°C
• Density: 1.055g/cm³
• Vapor Pressure: 0.00072mmHg at 25°C
• Refractive Index: 1.518
• CAS DataBase Reference: O-[3-(benzyloxy)propyl]hydroxylamine(CAS DataBase Reference)
• NIST Chemistry Reference: O-[3-(benzyloxy)propyl]hydroxylamine(114809-62-0)
• EPA Substance Registry System: O-[3-(benzyloxy)propyl]hydroxylamine(114809-62-0)

Safety Data

• Hazardous Substances Data: 114809-62-0(Hazardous Substances Data)

Upstream product

• 4799-68-2 3-benzyloxypropan-1-ol 
• 114809-45-9 N-<3-(benzyloxy)propoxy>phthalimide 

Downstream Products

• 114778-21-1 5-Amino-1-(3-benzyloxy-propoxy)-1H-imidazole-4-carboxylic acid amide 
• 116477-32-8 9(3-Benzyloxyprop-1-oxy)-6-chloro-2-formamidopurine 
• 114778-89-1 9-(3-benzyloxypropoxy)guanine 
• 114778-20-0 C₁₄H₁₈N₄O₃ 
• 118222-04-1 1-(3-Benzyloxypropoxy)-4-(1,2,4-triazol-1-yl)pyrimidin-2(1H)-one 
• 118222-01-8 1-(3-Benzyloxypropoxy)thymine 
• 118221-99-1 1-(3-Benzyloxypropoxy)uracil 
• 119080-68-1 1-(3-Benzyloxypropoxy)cytosine 
• 867168-92-1 2-amino-3-hydroxy-propionaldehyde O-(3-benzyloxy-propyl)-oxime 
• 116477-29-3 C₁₃H₂₀N₂O₂ 
• 118221-97-9 N-(3-Benzyloxypropoxy)urea 
• 116477-31-7 N-[4-(3-Benzyloxy-propoxyamino)-6-chloro-5-formylamino-pyrimidin-2-yl]-formamide 
• 123240-67-5 6-<<3-(benzyloxy)propoxy>amino>-4-chloro-5-formamidopyrimidine 

Relevant articles and documents

Method for synthesizing azanol

The invention relates to a hydroxylamine synthesis method. The hydroxylamine synthesis method comprises the following steps: (A) enabling alcohol to react with alkyl sulfonyl halide in the presence of an acid-binding agent to obtain sulphonate; (B) enabling the obtained sulphonate in the step (A) to react with N-hydroxycyclodiimide in the presence of alkali to generate alkylate of the N-hydroxycyclodiimide; and (C) enabling the alkylate obtained in the step (B) to react with an aminolysis reagent or a hydrazinolysis reagent to obtain the hydroxylamine. The method is high in yield and suitable for large-scale industrial hydroxylamine synthesis.

N3 ALKYLATED BENZIMIDAZOLE DERIVATIVES AS MEK INHIBITORS

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SYNTHESIS OF 9-(3-HYDROXYPROPOXY)GUANINE, A NOVEL ANTIVIRAL ACYCLONUCLEOSIDE

Synthetic approaches to 9-(3-hydroxypropoxy)guanine (2) involving the intermediacy of either a 1-alkoxyimidazole (7) or a 4-alkoxyaminopyrimidine (13) are described.This 9-alkoxyguanine (2) has potent and selective anti-herpesvirus activity and is the first reported member of a new series of antiviral acyclonucleosides.