Butanamide, 2-amino-N-(2-mercaptoethyl)-3-methyl-, monohydrobromide, (S)-

Base Information

Chemical Name:Butanamide, 2-amino-N-(2-mercaptoethyl)-3-methyl-, monohydrobromide, (S)-
CAS No.:120626-97-3
Molecular Formula:BrH*C₇H₁₆N₂OS
Molecular Weight:257.195
Hs Code.:
DSSTox Substance ID:DTXSID50152947

Synonyms:N-(2-Mercaptoethyl)valenamide hydrobromide;Valenamide, N-(2-mercaptoethyl)-, hydrobromide;Butanamide, 2-amino-N-(2-mercaptoethyl)-3-methyl-, monohydrobromide, (S)-;120626-97-3;C7H16N2OS.BrH;DTXSID50152947;C7-H16-N2-O-S.Br-H;LS-160875

Suppliers and Price of Butanamide, 2-amino-N-(2-mercaptoethyl)-3-methyl-, monohydrobromide, (S)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Butanamide, 2-amino-N-(2-mercaptoethyl)-3-methyl-, monohydrobromide, (S)-

Chemical Property:

Vapor Pressure:9.72E-05mmHg at 25°C
Boiling Point:338.6°Cat760mmHg
Flash Point:158.6°C
Density:g/cm³
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:256.02450
Heavy Atom Count:12
Complexity:128

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(C(=O)NCCS)N.Br
Isomeric SMILES:CC(C)[C@@H](C(=O)NCCS)N.Br

Technology Process of Butanamide, 2-amino-N-(2-mercaptoethyl)-3-methyl-, monohydrobromide, (S)-

There total 3 articles about Butanamide, 2-amino-N-(2-mercaptoethyl)-3-methyl-, monohydrobromide, (S)- 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: 90.0%

: 120627-06-7
carbobenzoxy-valinyl N-cysteamine

: 120626-97-3
(S)-2-Amino-N-(2-mercapto-ethyl)-3-methyl-butyramide; hydrobromide

Guidance literature:: With hydrogen bromide; In acetic acid; at -5 ℃; for 0.5h;
DOI:10.1016/0223-5234(88)90008-6

Reference yield:

: 126147-70-4
(2S)-3-Methyl-2-(phenoxycarbonyl)aminobutyric acid

: 120626-97-3
(S)-2-Amino-N-(2-mercapto-ethyl)-3-methyl-butyramide; hydrobromide

Guidance literature:: Multi-step reaction with 3 steps

1: DCC / tetrahydrofuran / 0 deg C, 30 min, RT, 3 h

2: sodium methylate / methanol / 1 h / Ambient temperature

3: 90 percent / HBr / acetic acid / 0.5 h / -5 °C

With hydrogen bromide; sodium methylate; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; acetic acid;
DOI:10.1016/0223-5234(88)90008-6

Reference yield:

: 120627-05-6
carbobenzoxy-valinyl-N-(S-acetyl)-cysteamine

: 120626-97-3
(S)-2-Amino-N-(2-mercapto-ethyl)-3-methyl-butyramide; hydrobromide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium methylate / methanol / 1 h / Ambient temperature

2: 90 percent / HBr / acetic acid / 0.5 h / -5 °C

With hydrogen bromide; sodium methylate; In methanol; acetic acid;
DOI:10.1016/0223-5234(88)90008-6