2,3-Dibromoallyl alcohol

Base Information

• Chemical Name: 2,3-Dibromoallyl alcohol
• CAS No.: 7228-11-7
• Molecular Formula: C3H4 Br2 O
• Molecular Weight: 215.872
• European Community (EC) Number: 230-629-8
• Nikkaji Number: J1.593.691F,J212.252I
• Wikidata: Q76324731
• Mol file: 7228-11-7.mol

Synonyms:2,3-Dibromo-2-propen-1-ol;2,3-Dibromoallyl alcohol;7228-11-7;(Z)-2,3-dibromoprop-2-en-1-ol;69298-57-3;EINECS 230-629-8;SCHEMBL4630846;(2Z)-2,3-Dibromo-2-propene-1-ol;2-Propen-1-ol,2,3-dibromo-,(2Z)-;2,3-Dibromo-2-propen-1-ol(cis and trans);2,3-Dibromo-2-propen-1-ol, technical, (cis+trans), >=90% (GC)

Chemical Property of 2,3-Dibromoallyl alcohol

Chemical Property:

• Vapor Pressure: 0.000305mmHg at 25°C
• Refractive Index: n20/D 1.581
• Boiling Point: 60-62 °C0.1 mm Hg(lit.)
• Flash Point: 71 °C
• PSA: 20.23000
• Density: 2.22 g/mL at 20 °C(lit.)
• LogP: 1.60990
• XLogP3: 1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 215.86084
• Heavy Atom Count: 6
• Complexity: 59.8

Purity/Quality:

98%,99%, ^*data from raw suppliers

2,3-Dibromo-2-propen-1-ol technical, (cis+trans), ≥90% (GC) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi,Xn
• Statements: 36/37/38-22
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C(C(=CBr)Br)O
• Isomeric SMILES: C(/C(=C/Br)/Br)O
• Uses: 2,3-Dibromo-2-propen-1-ol may be used in chemical synthesis.

Technology Process of 2,3-Dibromoallyl alcohol

There total 3 articles about 2,3-Dibromoallyl alcohol 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:

2,2,3-tribromo-propan-1-ol → 2,3-dibromo-prop-2-en-1-ol (7228-11-7)

Guidance literature:

With methanol; sodium;

Reference yield:

1,1,2-tribromo-propene (30980-32-6) → 2,3-dibromo-prop-2-en-1-ol (7228-11-7)

Guidance literature:

With potassium acetate; und Verseifung des so entstehenden Acetins;

Reference yield:

→ 2,3-dibromo-prop-2-en-1-ol (7228-11-7)

Guidance literature:

Prep.a) Carbontetrachloride, Propargylalcohol, Bromine;

upstream raw materials:

1,1,2-tribromo-propene