O-2-Propynylhydroxylamine hydrochloride

Base Information

• Chemical Name: O-2-Propynylhydroxylamine hydrochloride
• CAS No.: 21663-79-6
• Molecular Formula: C3H5NO.ClH
• Molecular Weight: 107.54
• Hs Code.: 2922199090
• European Community (EC) Number: 803-169-6
• DSSTox Substance ID: DTXSID00542379
• Mol file: 21663-79-6.mol

Synonyms:21663-79-6;O-2-Propynylhydroxylamine hydrochloride;O-Prop-2-ynyl-hydroxylamine hydrochloride;O-(prop-2-yn-1-yl)hydroxylamine hydrochloride;O-prop-2-ynylhydroxylamine;hydrochloride;Hydroxylamine, O-2-propynyl-, hydrochloride;Prop-2-ynyl-hydroxylamine;O-2-propynylhydroxylamne hcl;SCHEMBL874919;DTXSID00542379;O-Prop-2-ynyl-hydroxylamine HCl;CEFBXYRCGUITCZ-UHFFFAOYSA-N;CS-B1211;WAA66379;MFCD12912207;O-Propargylhydroxylamine hydrochloride;AKOS015969230;O-propargyl-hydroxylamine hydrochloride;SB35454;O-2-propynyl-hydroxylamine hydrochloride;o-Prop-2-ynylhydroxylamine hydrochloride;Prop-2-ynyl-hydroxylamine hydrochloride;BS-24982;O-(2-propynyl)hydroxylamine hydrochloride;O-(prop-2-ynyl)hydroxylamine hydrochloride;O-(prop-2-yn-1-yl)hydroxylaminehydrochloride;D77272;EN300-216214;A905247;J-014219;J-523815;O-2-Propynylhydroxylamine hydrochloride, AldrichCPR;O-Prop-2-yn-1-ylhydroxylamine--hydrogen chloride (1/1)

Chemical Property of O-2-Propynylhydroxylamine hydrochloride

Chemical Property:

• Melting Point: 148 - 150°C
• PSA: 35.25000
• LogP: 1.01220
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• Solubility.: DMSO (Slightly), Methanol (Slightly)
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 107.0137915
• Heavy Atom Count: 6
• Complexity: 51.2

Purity/Quality:

98%Min ^*data from raw suppliers

O-2-Propynylhydroxylamine hydrochloride ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xn
• Statements: 22

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C#CCON.Cl

Technology Process of O-2-Propynylhydroxylamine hydrochloride

There total 4 articles about O-2-Propynylhydroxylamine hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

2-(prop-2-yn-1-yloxy)isoindoline-1,3-dione (4616-63-1) → O-(prop-2-yn-1-yl)hydroxylamine hydrochloride (21663-79-6)

Guidance literature:

2-(prop-2-yn-1-yloxy)isoindoline-1,3-dione; With methylhydrazine; In dichloromethane; at 0 - 20 ℃; for 2h;

With hydrogenchloride; In 1,4-dioxane; at 0 ℃;

Reference yield: 86.0%

→ O-(prop-2-yn-1-yl)hydroxylamine hydrochloride (21663-79-6)

Guidance literature:

Reference yield:

→ (10Z)-8-(2-Dimethylaminoethoxy)-2,3-methylenedioxyindeno[1,2-b]indole-10(5H)-one O-(2-propynyl)oxime hydrochloride + O-(prop-2-yn-1-yl)hydroxylamine hydrochloride (21663-79-6)

Guidance literature:

upstream raw materials:

2-(prop-2-yn-1-yloxy)isoindoline-1,3-dione

Downstream raw materials:

E-(+/-)-1-azabicyclo[2.2.1]heptan-3-one, O-2-propynyloxime

Z-(+/-)-1-azabicyclo[2.2.1]heptan-3-one, O-2-propynyloxime

Refernces

• 1、 Banerjee, Deboshri,Liu, Allen P.,Voss, Neil R.,Schmid, Sandra L.,Finn. "Multivalent display and receptor-mediated endocytosis of transferrin on virus-like particles". . p. 1273 - 1279. Retrieved 2010.
• 2、 -. "With biological activity mixed oxygen benzene oxygen N- the oxygen radical is thick carboxylic acid amide compound and its preparation method". Paragraph 0071; 0072; 0074. . Retrieved 2016/10/08.