Methyl 2-[3-(phenylmethoxycarbonylamino)propanoylamino]acetate

Base Information

Chemical Name:Methyl 2-[3-(phenylmethoxycarbonylamino)propanoylamino]acetate
CAS No.:89137-40-6
Molecular Formula:C14H18N2O5
Molecular Weight:294.3031
Hs Code.:
NSC Number:164072
DSSTox Substance ID:DTXSID60304056
Wikidata:Q82049676

Synonyms:89137-40-6;methyl 2-[3-(phenylmethoxycarbonylamino)propanoylamino]acetate;DTXSID60304056;SRTRHRPTDAYVJN-UHFFFAOYSA-N;NSC164072;AKOS024338022;NSC-164072;N-carbobenzyloxy-.beta.-alanyl-glycine methyl ester;methyl [(3-{[(benzyloxy)carbonyl]amino}propanoyl)amino]acetate;Methyl [(3-([(benzyloxy)carbonyl]amino)propanoyl)amino]acetate #

Suppliers and Price of Methyl 2-[3-(phenylmethoxycarbonylamino)propanoylamino]acetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 4 raw suppliers

Chemical Property of Methyl 2-[3-(phenylmethoxycarbonylamino)propanoylamino]acetate

Chemical Property:

Vapor Pressure:1.47E-10mmHg at 25°C
Boiling Point:511°Cat760mmHg
Flash Point:262.9°C
Density:1.211g/cm³
XLogP3:0.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:9
Exact Mass:294.12157168
Heavy Atom Count:21
Complexity:353

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)CNC(=O)CCNC(=O)OCC1=CC=CC=C1

Technology Process of Methyl 2-[3-(phenylmethoxycarbonylamino)propanoylamino]acetate

There total 1 articles about Methyl 2-[3-(phenylmethoxycarbonylamino)propanoylamino]acetate 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:

: 2304-94-1
3-(benzyloxycarbonylamino)propanoic acid

: 5680-79-5,883886-67-7
glycine ethyl ester hydrochloride

: 89137-40-6
N-Carbobenzoxy-β-alanyl-glycin-methylester

Guidance literature:: With triethylamine; dicyclohexyl-carbodiimide; In chloroform;
DOI:10.1021/ja00844a046

Reference yield:

: 89137-40-6
N-Carbobenzoxy-β-alanyl-glycin-methylester

: 58171-88-3
Cbz-β-Ala-Gly-OH

Guidance literature:: With sodium hydroxide; In methanol;
DOI:10.1021/ja00844a046

Reference yield:

: 89137-40-6
N-Carbobenzoxy-β-alanyl-glycin-methylester

: 2672-88-0
β-alanylglycine

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH / methanol

2: H₂ / Pd-C / aq. ethanol; acetic acid

With sodium hydroxide; hydrogen; palladium on activated charcoal; In methanol; ethanol; acetic acid;
DOI:10.1021/ja00844a046