(2S,3S)-2-(tert-butoxycarbonylamino)-3-methylpentanal

Base Information

Chemical Name:(2S,3S)-2-(tert-butoxycarbonylamino)-3-methylpentanal
CAS No.:87694-55-1
Molecular Formula:C₁₁H₂₁NO₃
Molecular Weight:215.293
Hs Code.:
Nikkaji Number:J1.238.817I
Mol file:87694-55-1.mol

Synonyms:87694-55-1;(2S,3S)-2-(tert-butoxycarbonylamino)-3-methylpentanal;tert-butyl N-[(2S,3S)-3-methyl-1-oxopentan-2-yl]carbamate;N-Boc-2(S),3(S)-3-methylpentanal;N-(t-butyloxycarbonyl)-L-Isoleucinal;N-BOC-L-ISOLEUCINAL;N-t-Butoxycarbonyl isoleucinal;N-t-butoxycarbonyl-isoleucinal;SCHEMBL2520730;YJAAJMSZVZJPOQ-DTWKUNHWSA-N;N-(t-butoxycarbonyl)-L-Isoleucinal;MFCD00801200;MFCD09953266;AKOS030212098;AT12734;TS-7045;Boc-L-Ile-PAM resin (100-200 mesh);tert-butyl ((2S,3S)-3-methyl-1-oxopentan-2-yl)carbamate;((1S,2S)-1-formyl-2-methyl-butyl)-carbamic acid tert-butyl ester;Boc-L-isoleucine Merrifield resin 100-200 Mesh, 0.3-1.2 meq/g 1% DVB

Suppliers and Price of (2S,3S)-2-(tert-butoxycarbonylamino)-3-methylpentanal

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

Total 6 raw suppliers

Chemical Property of (2S,3S)-2-(tert-butoxycarbonylamino)-3-methylpentanal

Chemical Property:

PSA：55.40000
LogP:2.51560
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:215.15214353
Heavy Atom Count:15
Complexity:220

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(C)C(C=O)NC(=O)OC(C)(C)C
Isomeric SMILES:CC[C@H](C)[C@@H](C=O)NC(=O)OC(C)(C)C

Technology Process of (2S,3S)-2-(tert-butoxycarbonylamino)-3-methylpentanal

There total 23 articles about (2S,3S)-2-(tert-butoxycarbonylamino)-3-methylpentanal 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%

: 87694-51-7
N-(tert-butoxycarbonyl)-L-isoleucine N'-methoxy-N'-methylamide

: 118171-79-2,141321-51-9,141321-54-2,87694-55-1
N-(t-butoxycarbonyl)-isoleucine aldehyde

Guidance literature:: With lithium aluminium tetrahydride; at 0 ℃; for 0.25h;
DOI:10.1081/NCN-100002563

Reference yield: 97.0%

: 141321-52-0,141321-53-1,141321-50-8,106946-74-1,545433-88-3
N-(tert-butoxycarbonyl)-L-isoleucinol

: 118171-79-2,141321-51-9,141321-54-2,87694-55-1
N-(t-butoxycarbonyl)-isoleucine aldehyde

Guidance literature:: With sulfur trioxide pyridine complex; dimethyl sulfoxide; triethylamine; In dichloromethane; at -10 ℃;
DOI:10.1016/j.bmcl.2003.09.088