(2-Bromo-Propionylamino)-Acetic Acid

Base Information

• Chemical Name: (2-Bromo-Propionylamino)-Acetic Acid
• CAS No.: 25413-03-0
• Molecular Formula: C5H8 Br N O3
• Molecular Weight: 210.027
• Hs Code.: 2924199090
• European Community (EC) Number: 651-978-6
• NSC Number: 163101
• Nikkaji Number: J21.926F
• Mol file: 25413-03-0.mol

Synonyms:(2-Bromo-Propionylamino)-Acetic Acid;25413-03-0;2-(2-bromopropanoylamino)acetic acid;NSC163101;SCHEMBL9146654;D,L-2-BROMOPROPIONYLGLYCINE;AKOS022506142;NSC-163101

Chemical Property of (2-Bromo-Propionylamino)-Acetic Acid

Chemical Property:

• Vapor Pressure: 5.55E-08mmHg at 25°C
• Boiling Point: 413.1°Cat760mmHg
• Flash Point: 203.6°C
• PSA: 66.40000
• Density: 1.677g/cm³
• LogP: 0.36150
• XLogP3: 0.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 208.96876
• Heavy Atom Count: 10
• Complexity: 148

Purity/Quality:

99%min ^*data from raw suppliers

(2-Bromopropionylamino)aceticAcid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(C(=O)NCC(=O)O)Br

Technology Process of (2-Bromo-Propionylamino)-Acetic Acid

There total 4 articles about (2-Bromo-Propionylamino)-Acetic Acid 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:

ethyl 2-(2-bromopropanamido)acetate (25413-02-9) → N-(2-bromo-propionyl)-glycine (25413-03-0)

Guidance literature:

-aminoacetic acid; durch Verseifen;

Reference yield:

glycine (56-40-6,18875-39-3,25718-94-9) → N-(2-bromo-propionyl)-glycine (25413-03-0)

Guidance literature:

With sodium hydroxide; -aminoacetic acid;

Reference yield:

(R)-2-bromopropionyl chloride (7148-74-5,22592-73-0,71425-59-7,52152-04-2) + glycine (56-40-6,18875-39-3,25718-94-9) → N-(2-bromo-propionyl)-glycine (25413-03-0)

Guidance literature:

With sodium hydroxide; -aminoacetic acid;

upstream raw materials:

ethyl 2-(2-bromopropanamido)acetate

α-bromopropionyl bromide

glycine

(R)-2-bromopropionyl chloride

Downstream raw materials:

L-Lactic acid

N-(2-mercaptopropionyl)glycine

D-ala-gly

alanylglycine