2-{1-[(tert-butoxy)carbonyl]-2,3-dihydro-1H-indol-3-yl}acetic acid

Base Information

Chemical Name:2-{1-[(tert-butoxy)carbonyl]-2,3-dihydro-1H-indol-3-yl}acetic acid
CAS No.:1321843-22-4
Molecular Formula:C₁₅H₁₉NO₄
Molecular Weight:277.32
Hs Code.:
European Community (EC) Number:886-604-2

Synonyms:1321843-22-4;2-{1-[(tert-butoxy)carbonyl]-2,3-dihydro-1H-indol-3-yl}acetic acid;2-[1-[(2-methylpropan-2-yl)oxycarbonyl]-2,3-dihydroindol-3-yl]acetic acid;2-(1-[(TERT-BUTOXY)CARBONYL]-2,3-DIHYDRO-1H-INDOL-3-YL)ACETIC ACID;SCHEMBL3956185;PPVKBEWRGPFIIJ-UHFFFAOYSA-N;(1-t-butoxycarbonyl-2,3-dihydro-1H-indol-3-yl)acetic acid;MFCD21983583;AKOS019067213;BS-45529;DB-361882;E84335;EN300-107189;2-{1-Boc-2,3-dihydro-1H-indol-3-yl}acetic Acid;Z1413723812;[1-(tert-butoxycarbonyl)-2,3-dihydroindol-3-yl]acetic acid;(+)-(1-tert-Butoxycarbonyl-2,3-dihydro-1H-indol-3-yl)acetic acid;2-{1-[(tert-butoxy)carbonyl]-2,3-dihydro-1H-indol-3-yl}aceticacid

Suppliers and Price of 2-{1-[(tert-butoxy)carbonyl]-2,3-dihydro-1H-indol-3-yl}acetic acid

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
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Total 2 raw suppliers

Chemical Property of 2-{1-[(tert-butoxy)carbonyl]-2,3-dihydro-1H-indol-3-yl}acetic acid

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:277.13140809
Heavy Atom Count:20
Complexity:388

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)OC(=O)N1CC(C2=CC=CC=C21)CC(=O)O

Technology Process of 2-{1-[(tert-butoxy)carbonyl]-2,3-dihydro-1H-indol-3-yl}acetic acid

There total 5 articles about 2-{1-[(tert-butoxy)carbonyl]-2,3-dihydro-1H-indol-3-yl}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: 40.0%

: 124-38-9,18923-20-1
carbon dioxide

: 161361-83-7
N-allyl-N-(t-butoxycarbonyl)-2-bromoaniline

: 1321843-22-4
(1-t-butoxycarbonyl-2,3-dihydro-1H-indol-3-yl)acetic acid

Guidance literature:: With methyl 4-tert-butylbenzoate; tetrabutylammonium tetrafluoroborate; In N,N-dimethyl-formamide; at 0 ℃; Electrolysis;
DOI:10.1055/s-0030-1260794

Reference yield:

: 926028-90-2
t-butyl (R)-3-(2-methoxy-2-oxoethyl)indoline-1-carboxylate

: 1321843-22-4
(-)-(R)-(1-tert-butoxycarbonyl-2,3-dihydro-1H-indol-3-yl)acetic acid

Guidance literature:: t-butyl (R)-3-(2-methoxy-2-oxoethyl)indoline-1-carboxylate; With sodium hydroxide; ethanol; water; at 20 ℃; for 0.5h;

In ethanol; water; pH=1;