Boc-Ala-OH-15N

Base Information

Chemical Name:Boc-Ala-OH-15N
CAS No.:139952-87-7
Molecular Formula:C8H15NO4
Molecular Weight:190.22
Hs Code.:
DSSTox Substance ID:DTXSID40498922
Wikidata:Q72510560
Mol file:139952-87-7.mol

Synonyms:139952-87-7;Boc-Ala-OH-15N;Boc-L-Ala-OH-15N;(2S)-2-[(2-Methylpropan-2-yl)oxycarbonyl(15N)amino]propanoic acid;N-(tert-Butoxycarbonyl)-L-(~15~N)alanine;DTXSID40498922;HY-41121S4;CS-0376603;Boc-Ala-OH-15N, >=98 atom % 15N, >=99% (CP)

Suppliers and Price of Boc-Ala-OH-15N

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

Sigma-Aldrich
Boc-Ala-OH-15N 98 atom %
250mg
$ 286.00

Medical Isotopes, Inc.
L-Alanine-15N-N-t-BOC
1 g
$ 810.00

American Custom Chemicals Corporation
L-ALANINE-15N-N-T-BOC 95.00%
1G
$ 861.05

Total 9 raw suppliers

Chemical Property of Boc-Ala-OH-15N

Chemical Property:

Melting Point:79-83 °C(lit.)
PSA：75.63000
LogP:1.37510
Storage Temp.:-15°C
XLogP3:0.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:190.09714285
Heavy Atom Count:13
Complexity:207

Purity/Quality:

97% ^*data from raw suppliers

Boc-Ala-OH-15N 98 atom % ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C(=O)O)NC(=O)OC(C)(C)C
Isomeric SMILES:C[C@@H](C(=O)O)[15NH]C(=O)OC(C)(C)C
Uses L-Alanine-15N-N-t-BOC (CAS# 139952-87-7) is a useful isotopically labeled research compound. BOC-[15N]ALA-OH can be synthesized from chiral alpha-hydroxy acids. Gradiently enriching BOC-[15N]ALA-OH also helps provide insights into glycoprotein behavior.

Technology Process of Boc-Ala-OH-15N

There total 1 articles about Boc-Ala-OH-15N 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:

: 139929-04-7
benzyl (S)-N-(t-butoxycarbonyl)<15N>alaninate

: 139952-87-7
[15N]-N-(tert-butoxycarbonyl)-L-alanine

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; under 1 Torr;

Reference yield: 3.0%

: 15761-39-4,59433-50-0
1-(tert-butoxycarbonyl)-L-proline

: 13734-41-3
t-Boc-L-valine

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

: 7536-55-2
N-tert-butyloxycarbonylasparagine

: 7536-58-5,98482-77-0
BOC-L-aspartic acid 4-benzyl ester

: 13726-85-7
Boc-Gln-OH

: 13574-13-5
Boc-Glu(OBzl)-OH

: 120267-95-0
Boc-Arg(Z)2-OH

: 18942-46-6,58290-35-0
N-(tert-butyloxycarbonyl)-S-(4-methoxybenzyl)cysteine

: C₂₄H₂₉N₂O₆Pol

: 54613-99-9
Boc-(S)-Lys(2-Cl-Z)-OH

: 47355-10-2
Nα-tert-butoxycarbonyl-1-formyl-L-tryptophan

: 139952-87-7
[15N]-N-(tert-butoxycarbonyl)-L-alanine

: 141509-91-3
(15N)-N^α-t-Boc-L-valine

: C₁₄H₁₉⁽¹⁵⁾NO₄

: C₁₂₃H₁₉₈N₃₂⁽¹⁵⁾N₄O₃₆S

Guidance literature:: N-tert-butyloxycarbonylasparagine; C₂₄H₂₉N₂O₆Pol; With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; for 0.2h;

With trifluoroacetic acid; In N,N-dimethyl-formamide;

1-(tert-butoxycarbonyl)-L-proline; t-Boc-L-valine; N-tert-butoxycarbonyl-L-leucine; N-tert-butyloxycarbonylasparagine; BOC-L-aspartic acid 4-benzyl ester; Boc-Gln-OH; Boc-Glu(OBzl)-OH; Boc-Arg(Z)2-OH; N-(tert-butyloxycarbonyl)-S-(4-methoxybenzyl)cysteine; Boc-(S)-Lys(2-Cl-Z)-OH; Nα-tert-butoxycarbonyl-1-formyl-L-tryptophan; [15N]-N-(tert-butoxycarbonyl)-L-alanine; (15N)-N^α-t-Boc-L-valine; C₁₄H₁₉⁽¹⁵⁾NO₄; Further stages;
DOI:10.1021/jacs.7b03277