O-Allylhydroxylamine hydrochloride hydrate

Base Information

• Chemical Name: O-Allylhydroxylamine hydrochloride hydrate
• CAS No.: 206557-03-1
• Molecular Formula: C₃H₇NO*ClH*H₂O
• Molecular Weight: 127.571
• Hs Code.: 2922199090
• European Community (EC) Number: 630-437-8,689-576-8
• DSSTox Substance ID: DTXSID20583466
• Mol file: 206557-03-1.mol

Synonyms:O-Allylhydroxylamine hydrochloride hydrate;206557-03-1;O-prop-2-enylhydroxylamine;hydrate;hydrochloride;SCHEMBL3917047;DTXSID20583466;VYCHJEXJHFTAQI-UHFFFAOYSA-N;O-allyl hydroxylamine hydrochloride hydrate;o-allylhydroxylamine hydrochloride monohydrate;O-Allylhydroxylamine hydrochloride hydra te,97%;O-Allylhydroxylamine hydrochloride hydrate, 97%;O-Prop-2-en-1-ylhydroxylamine--hydrogen chloride--water (1/1/1)

Chemical Property of O-Allylhydroxylamine hydrochloride hydrate

Chemical Property:

• Vapor Pressure: 0.00211mmHg at 25°C
• Melting Point: 175 °C (dec.)(lit.)
• Boiling Point: 265.2oC at 760 mmHg
• Flash Point: 114.2oC
• PSA: 44.48000
• LogP: 1.50070
• Solubility.: methanol: soluble25mg/mL, clear, colorless
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 127.0400063
• Heavy Atom Count: 7
• Complexity: 28.1

Purity/Quality:

98%Min ^*data from raw suppliers

O-Allylhydroxylamine hydrochloride hydrate ^*data from reagent suppliers

Safty Information:

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-27-28-36/37/39-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CCON.O.Cl
• Uses: O-Allylhydroxylamine hydrochloride hydrate has been used in the preparation of acetophenone O-allyloxime and O-allyI-N-(2-trimethylsilylethyloxycarbonyl)-hydroxylamine.

Technology Process of O-Allylhydroxylamine hydrochloride hydrate

There total 1 articles about O-Allylhydroxylamine hydrochloride hydrate 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:

→ O-allyl-hydroxylamine hydrochloride monohydrate (206557-03-1)

Guidance literature:

Refernces

• 1、 -. "Benzenesulfonamide derivatives and their use as MEK inhibitors". . . Retrieved 2008/06/13.