Me-Aib-OH*HCl

Base Information

Chemical Name:Me-Aib-OH*HCl
CAS No.:1223405-15-9
Molecular Formula:C₅H₁₁NO₂*ClH
Molecular Weight:153.609
Hs Code.:29224999

Synonyms:

Suppliers and Price of Me-Aib-OH*HCl

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

TRC
N-Me-Aib-OHhydrochloride
1g
$ 75.00

Crysdot
2-Methyl-2-(methylamino)propanoicacidhydrochloride 95+%
25g
$ 1250.00

Crysdot
2-Methyl-2-(methylamino)propanoicacidhydrochloride 95+%
10g
$ 624.00

Crysdot
2-Methyl-2-(methylamino)propanoicacidhydrochloride 95+%
5g
$ 356.00

Crysdot
2-Methyl-2-(methylamino)propanoicacidhydrochloride 95+%
1g
$ 129.00

AK Scientific
2-Methyl-2-(methylamino)propanoicacidhydrochloride
2.5g
$ 127.00

AK Scientific
2-Methyl-2-(methylamino)propanoicacidhydrochloride
250mg
$ 125.00

AK Scientific
2-Methyl-2-(methylamino)propanoicacidhydrochloride
10g
$ 198.00

AK Scientific
2-Methyl-2-(methylamino)propanoicacidhydrochloride
5g
$ 149.00

Total 2 raw suppliers

Chemical Property of Me-Aib-OH*HCl

Chemical Property:

Purity/Quality:

95+% ^*data from raw suppliers

N-Me-Aib-OHhydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses N-Me-Aib-OH HCl

Technology Process of Me-Aib-OH*HCl

There total 2 articles about Me-Aib-OH*HCl 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:

: 146000-39-7
N-tert-butoxycarbonyl-N-methyl-α-aminoisobutyric acid

: 1223405-15-9
Me-Aib-OH*HCl

Guidance literature:: N-tert-butoxycarbonyl-N-methyl-α-aminoisobutyric acid; With trifluoroacetic acid; In dichloromethane; water; at 20 ℃; for 6.5h;

With hydrogenchloride; In diethyl ether; at 20 ℃; for 0.0833333h;
DOI:10.1021/acs.orglett.9b01580

Reference yield:

: methyl 2-((tert-butoxycarbonyl)(methyl)amino)-2-methylpropanoate

: 1223405-15-9
Me-Aib-OH*HCl

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium hydroxide; water / 1,4-dioxane / 42 h / 50 °C

2.1: trifluoroacetic acid / dichloromethane; water / 6.5 h / 20 °C

2.2: 0.08 h / 20 °C

With water; trifluoroacetic acid; lithium hydroxide; In 1,4-dioxane; dichloromethane; water;
DOI:10.1021/acs.orglett.9b01580