2-Amino-N-(2-amino-2-oxoethyl)-4-methylpentanamide;hydrochloride

Base Information

Chemical Name:2-Amino-N-(2-amino-2-oxoethyl)-4-methylpentanamide;hydrochloride
CAS No.:38173-66-9
Molecular Formula:C8H17 N3 O2 . Cl H
Molecular Weight:223.703
Hs Code.:
DSSTox Substance ID:DTXSID40585164
NSC Number:523371
Mol file:38173-66-9.mol

Synonyms:2-Amino-N-(2-amino-2-oxoethyl)-4-methylpentanamide;hydrochloride;DTXSID40585164;NSC523371;NSC-523371;Leucylglycinamide--hydrogen chloride (1/1)

Suppliers and Price of 2-Amino-N-(2-amino-2-oxoethyl)-4-methylpentanamide;hydrochloride

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

Crysdot
(S)-2-(2-Aminoacetamido)-4-methylpentanamidehydrochloride 97%
10g
$ 406.00

American Custom Chemicals Corporation
GLY-LEU AMIDE HYDROCHLORIDE 98.00%
25G
$ 1732.50

American Custom Chemicals Corporation
GLY-LEU AMIDE HYDROCHLORIDE 98.00%
5G
$ 1530.38

American Custom Chemicals Corporation
GLY-LEU AMIDE HYDROCHLORIDE 98.00%
1G
$ 206.85

AK Scientific
Gly-Leuamidehydrochloride
1g
$ 110.00

Total 10 raw suppliers

Chemical Property of 2-Amino-N-(2-amino-2-oxoethyl)-4-methylpentanamide;hydrochloride

Chemical Property:

PSA：98.21000
LogP:1.55480
Storage Temp.:−20°C
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:223.1087545
Heavy Atom Count:14
Complexity:192

Purity/Quality:

99% ^*data from raw suppliers

(S)-2-(2-Aminoacetamido)-4-methylpentanamidehydrochloride 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)CC(C(=O)NCC(=O)N)N.Cl

Technology Process of 2-Amino-N-(2-amino-2-oxoethyl)-4-methylpentanamide;hydrochloride

There total 2 articles about 2-Amino-N-(2-amino-2-oxoethyl)-4-methylpentanamide;hydrochloride 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: 100.0%

: 89226-19-7
tert-butyloxycarbonylleucyl-glycine amide

: 38173-66-9
HCl_.H-Leu-Gly-NH₂

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 0.666667h;
DOI:10.1016/j.ejmech.2012.12.041

Reference yield:

: 13139-15-6,53296-34-7
N-tert-butoxycarbonyl-L-leucine

: 38173-66-9
HCl_.H-Leu-Gly-NH₂

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / dichloromethane / 0.17 h

1.2: 20 °C

2.1: hydrogenchloride / 1,4-dioxane / 0.67 h / 20 °C

With hydrogenchloride; triethylamine; In 1,4-dioxane; dichloromethane;
DOI:10.1016/j.ejmech.2012.12.041

Reference yield:

: 38173-66-9
HCl_.H-Leu-Gly-NH₂

: 2002-44-0
melanostatin

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine (TEA) / CH₂Cl₂; CHCl₃ / 1.) -7 deg C, 1 h, 2.) 0 deg C, 18 h

2: 80 percent / H₂ / Pd / ethanol

With hydrogen; triethylamine; palladium; In ethanol; dichloromethane; chloroform;
DOI:10.1007/BF00630256