Asn-Gly

Base Information

Chemical Name:Asn-Gly
CAS No.:67576-72-1
Molecular Formula:C6H11N3O4
Molecular Weight:189.171
Hs Code.:
DSSTox Substance ID:DTXSID40432523
Nikkaji Number:J36.186K
Wikidata:Q27140507
Metabolomics Workbench ID:78703

Synonyms:Asn-Gly;asparaginyl-glycine;67576-72-1;NG dipeptide;Asparaginylglycine;Asparagylmonoglycin;N-G Dipeptide;L-asparaginylglycine;L-Asn-Gly;L-Asparaginyl-glycine;N-L-Asparaginylglycine;L-Asparaginyl-L-Glycine;Asparagine Glycine dipeptide;Asparagine-Glycine dipeptide;SCHEMBL16685;CHEBI:73422;DTXSID40432523;Q27140507;N-G

Suppliers and Price of Asn-Gly

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 2 raw suppliers

Chemical Property of Asn-Gly

Chemical Property:

XLogP3:-5.2
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:189.07495584
Heavy Atom Count:13
Complexity:228

Purity/Quality:: ≥95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C(C(C(=O)NCC(=O)O)N)C(=O)N
Isomeric SMILES:C([C@@H](C(=O)NCC(=O)O)N)C(=O)N

Technology Process of Asn-Gly

There total 3 articles about Asn-Gly 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:

: 55247-97-7
(S)-N-[Bis-(4-methoxy-phenyl)-methyl]-2-tert-butoxycarbonylamino-succinamic acid

: 67576-72-1
L-asparaginylglycine

: 3790-51-0
aspartylglycine

Guidance literature:: With dicyclohexyl-carbodiimide; trifluoroacetic acid; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; 2.) CH₂Cl₂, 25 deg C, 40 min.;
DOI:10.1021/jo01292a001

Reference yield:

: 64817-62-5
t-butoxycarbonyl-L-asparagine anhydride

: 67576-72-1
L-asparaginylglycine

: 3790-51-0
aspartylglycine

: 72378-51-9
β-cyanoalanylglycine

: 72378-49-5
β-aspartamidinoacetic acid

Guidance literature:: With trifluoroacetic acid; Yield given. Multistep reaction. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; 1.) 25 deg C, 20 min., 2.) CH₂Cl₂, 25 deg C, 40 min.;
DOI:10.1021/jo01292a001

Reference yield:

: 64817-62-5
t-butoxycarbonyl-L-asparagine anhydride

: 67576-72-1
L-asparaginylglycine

: 3790-52-1
NSC 186908

: 72378-51-9
β-cyanoalanylglycine

: 72378-49-5
β-aspartamidinoacetic acid

Guidance literature:: With trifluoroacetic acid; Yield given. Multistep reaction. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; 1.) 25 deg C, 20 min., 2.) CH₂Cl₂, 25 deg C, 40 min.;
DOI:10.1021/jo01292a001