Tert-butyl 1,3-DI(methoxycarbonyl)propylcarbamate

Base Information

Chemical Name:Tert-butyl 1,3-DI(methoxycarbonyl)propylcarbamate
CAS No.:861658-15-3
Molecular Formula:C₁₂H₂₁NO₆
Molecular Weight:275.302
Hs Code.:
European Community (EC) Number:875-153-7

Synonyms:861658-15-3;TERT-BUTYL 1,3-DI(METHOXYCARBONYL)PROPYLCARBAMATE;Dimethyl 2-((tert-butoxycarbonyl)amino)pentanedioate;dimethyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanedioate;MFCD03094773;MFCD03094774;N-Boc-L-glutamic acid 1,5-dimethyl ester;DIMETHYL-N-TERT-BUTOXY-CARBONYL-GLUTAMATE;2,6-Dimethylisonicotinic?acid;SCHEMBL2225458;BCP30716;AB6641;MFCD02179298;AKOS027339516;MB02312;AS-44792;SY041419;SY258926;N-Boc-D-glutamic Acid 1,5-Dimethyl Ester;CS-0526941;FT-0630000;EN300-749184;A832238;Dimethyl2-((tert-butoxycarbonyl)amino)pentanedioate;1,5-dimethyl 2-{[(tert-butoxy)carbonyl]amino}pentanedioate;2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]pentanedioic acid dimethyl ester;N-Boc-L-Glutamic Acid dimethyl ester;Boc-Glu(OMe)-OMe;(S)-Dimethyl 2-((tert-butoxycarbonyl)amino)pentanedioate

Suppliers and Price of Tert-butyl 1,3-DI(methoxycarbonyl)propylcarbamate

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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price

Total 2 raw suppliers

Chemical Property of Tert-butyl 1,3-DI(methoxycarbonyl)propylcarbamate

Chemical Property:

XLogP3:1.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:9
Exact Mass:275.13688739
Heavy Atom Count:19
Complexity:334

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC(CCC(=O)OC)C(=O)OC

Technology Process of Tert-butyl 1,3-DI(methoxycarbonyl)propylcarbamate

There total 31 articles about Tert-butyl 1,3-DI(methoxycarbonyl)propylcarbamate 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: 100.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 23150-65-4
L-glutamic dimethyl ester hydrochloride

: 59279-60-6,130622-05-8,861658-15-3
dimethyl (2S)-2-[(tert-butoxycarbonyl)amino]pentanedioate

Guidance literature:: With sodium hydrogencarbonate; In tetrahydrofuran; water; at 20 ℃; for 16h; Inert atmosphere;
DOI:10.1002/anie.201402259

Reference yield: 98.0%

: 67-56-1
methanol

: 56-86-0,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6
L-glutamic acid

: 24424-99-5
di-tert-butyl dicarbonate

: 59279-60-6,130622-05-8,861658-15-3
dimethyl (2S)-2-[(tert-butoxycarbonyl)amino]pentanedioate

Guidance literature:: methanol; L-glutamic acid; With chloro-trimethyl-silane; at 0 - 20 ℃;

di-tert-butyl dicarbonate; With triethylamine; for 3h;
DOI:10.1002/anie.201803849