2-(2-((tert-Butoxycarbonyl)amino)ethoxy)acetic acid

Base Information Edit

Chemical Name:2-(2-((tert-Butoxycarbonyl)amino)ethoxy)acetic acid
CAS No.:142929-49-5
Molecular Formula:C9H17NO5
Molecular Weight:219.238
Hs Code.:2924199090
European Community (EC) Number:818-569-6
DSSTox Substance ID:DTXSID40566756
Wikidata:Q72448315
Mol file:142929-49-5.mol

Synonyms:142929-49-5;2-(2-((tert-Butoxycarbonyl)amino)ethoxy)acetic acid;t-Boc-N-amido-PEG1-CH2CO2H;N-Boc-2-(2-aminoethoxy)acetic Acid;(2-Boc-Aminoethoxy)acetic acid;BocNH-PEG1-CH2COOH;Boc-NH-PEG1-CH2COOH;2-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethoxy]acetic acid;MFCD09909935;Acetic acid, [2-[[(1,1-dimethylethoxy)carbonyl]amino]ethoxy]-;2-(2-([(tert-Butoxy)carbonyl]amino)ethoxy)acetic acid;2-(2-{[(tert-butoxy)carbonyl]amino}ethoxy)acetic acid;{2-[(TERT-BUTOXYCARBONYL)AMINO]ETHOXY}ACETIC ACID;t-boc-N-amido-PEG1-acetic acid;Boc-5-Amino-3-oxapentanoic acid;(2-Boc-amino-ethoxy)-acetic acid;SCHEMBL320644;(2-Boc-amino-ethoxy)acetic acid;DTXSID40566756;t-Boc-N-Amido-PEG1-CH2COOH;UPBQMAHYLWJGDW-UHFFFAOYSA-N;N-Boc-(2-aminoethoxy)acetic acid;Acetic acid, 2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]ethoxy]-;AKOS015908991;FS-5758;AC-26585;AM808137;BP-22041;SY033318;HY-140476;CS-0115466;5-tert.-butoxycarbonylamino-3-oxavaleric acid;EN300-74705;F52563;5-(t-butyloxycarbonyl-amino)-3-oxapentanoic acid;A807986;Z1171159734;2-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethoxy]ethanoic acid;2-[2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]ethoxy]acetic acid;Aceticacid,[2-[[(1,1-dimethylethoxy)carbonyl]amino]ethoxy]-(9CI)

Suppliers and Price of 2-(2-((tert-Butoxycarbonyl)amino)ethoxy)acetic acid

Supply Marketing:Edit

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
2-(2-((tert-Butoxycarbonyl)amino)ethoxy)aceticAcid
50mg
$ 60.00

SynQuest Laboratories
N-Boc-(2-aminoethoxy)acetic acid 97.0%
5 g
$ 395.00

SynQuest Laboratories
N-Boc-(2-aminoethoxy)acetic acid 97.0%
250 mg
$ 55.00

SynQuest Laboratories
N-Boc-(2-aminoethoxy)acetic acid 97.0%
1 g
$ 125.00

purepeg
BocNH-PEG1-CH2COOH min.95%
5 g
$ 248.00

Oakwood
(2-Boc-Aminoethoxy)acetic acid
250mg
$ 30.00

Oakwood
(2-Boc-Aminoethoxy)acetic acid
1g
$ 73.00

Oakwood
(2-Boc-Aminoethoxy)acetic acid
5g
$ 285.00

Iris Biotech GmbH
Boc-O1Pen-OH*DCHA
25 g
$ 1080.00

Iris Biotech GmbH
Boc-O1Pen-OH*DCHA
5 g
$ 270.00

Total 34 raw suppliers

Chemical Property of 2-(2-((tert-Butoxycarbonyl)amino)ethoxy)acetic acid Edit

Chemical Property:

Vapor Pressure:3.3E-07mmHg at 25°C
Refractive Index:1.462
Boiling Point:391.2 °C at 760 mmHg
PKA:3.44±0.10(Predicted)
Flash Point:190.4 °C
PSA：84.86000
Density:1.151 g/cm³
LogP:1.00320
Storage Temp.:-20°C
XLogP3:0.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:7
Exact Mass:219.11067264
Heavy Atom Count:15
Complexity:221

Purity/Quality:

98%,99%, ^*data from raw suppliers

2-(2-((tert-Butoxycarbonyl)amino)ethoxy)aceticAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NCCOCC(=O)O
Description t-Boc-N-amido-PEG1-CH2CO2H is a PEG linker containing a terminal carboxylic acid and Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Uses This is a crosslinker with a t-Boc protected amine on one end and a carboxyl group on the other end. The compound contains a single PEG unit to help improve solubility

Technology Process of 2-(2-((tert-Butoxycarbonyl)amino)ethoxy)acetic acid

There total 7 articles about 2-(2-((tert-Butoxycarbonyl)amino)ethoxy)acetic 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: 99.0%