Caproyl glutamic acid

Base Information

Chemical Name:Caproyl glutamic acid
CAS No.:111276-71-2
Molecular Formula:C15H27NO5
Molecular Weight:301.37900
Hs Code.:
UNII:I6YHE9T07Q
DSSTox Substance ID:DTXSID10149575
Nikkaji Number:J3.537.739E
Wikidata:Q27280513
Mol file:111276-71-2.mol

Synonyms:Caproyl glutamic acid;111276-71-2;N-Decanoyl-l-glutamic acid;N-Decanoylglutamic acid;UNII-I6YHE9T07Q;L-Glutamic acid, N-(1-oxodecyl)-;I6YHE9T07Q;(2S)-2-(decanoylamino)pentanedioic acid;SCHEMBL342881;DTXSID10149575;(S)-2-Decanamidopentanedioic acid;Q27280513

Suppliers and Price of Caproyl glutamic acid

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 Caproyl glutamic acid

Chemical Property:

PSA：107.19000
LogP:3.40160
XLogP3:3.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:13
Exact Mass:301.18892296
Heavy Atom Count:21
Complexity:330

Purity/Quality:: 95%+ or 98%+ ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCC(=O)NC(CCC(=O)O)C(=O)O
Isomeric SMILES:CCCCCCCCCC(=O)N[C@@H](CCC(=O)O)C(=O)O

Technology Process of Caproyl glutamic acid

There total 6 articles about Caproyl glutamic 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:

: 18735-78-9
2,5-diphenyloxazole-4-carboxylic acid

: 112-13-0
n-decanoyl chloride

: 133464-46-7
(S)-2-[((9H-fluoren-9-yl)methoxy)carbonylamino]-5-(allyloxy)-5-oxopentanoic acid

: 289905-94-8
N-allyloxycarbonyl-N'-benzylethylenediamine

: 111276-71-2
N^α-decanoyl-L-glutamic acid

: (S)-4-(Benzyl-{2-[(2,5-diphenyl-oxazole-4-carbonyl)-amino]-ethyl}-carbamoyl)-2-decanoylamino-butyric acid

Guidance literature:: Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1016/S0968-0896(96)00199-X

Reference yield:

: 18735-78-9
2,5-diphenyloxazole-4-carboxylic acid

: 112-13-0
n-decanoyl chloride

: 133464-46-7
(S)-2-[((9H-fluoren-9-yl)methoxy)carbonylamino]-5-(allyloxy)-5-oxopentanoic acid

: 188403-10-3
(2-Methylamino-ethyl)-carbamic acid allyl ester

: 111276-71-2
N^α-decanoyl-L-glutamic acid

: (S)-2-Decanoylamino-4-({2-[(2,5-diphenyl-oxazole-4-carbonyl)-amino]-ethyl}-methyl-carbamoyl)-butyric acid

Guidance literature:: Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1016/S0968-0896(96)00199-X

Reference yield:

: 18735-78-9
2,5-diphenyloxazole-4-carboxylic acid

: 112-13-0
n-decanoyl chloride

: 133464-46-7
(S)-2-[((9H-fluoren-9-yl)methoxy)carbonylamino]-5-(allyloxy)-5-oxopentanoic acid

: (2-Hexylamino-ethyl)-carbamic acid allyl ester

: 111276-71-2
N^α-decanoyl-L-glutamic acid

: (S)-2-Decanoylamino-4-({2-[(2,5-diphenyl-oxazole-4-carbonyl)-amino]-ethyl}-hexyl-carbamoyl)-butyric acid

Guidance literature:: Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1016/S0968-0896(96)00199-X