Structure

N,N'-Di-tert-butoxycarbonyl-L-histidine

CAS
20866-46-0
Catalog Number
ACM20866460
Category
Other Products
Molecular Weight
355.39
Molecular Formula
C16H25N3O6

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Specification

Synonyms
Boc-His(Boc)-OH, 20866-46-0, N,N-Di-tert-butoxycarbonyl-L-histidine, (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[1-[(2-methylpropan-2-yl)oxycarbonyl]imidazol-4-yl]propanoic acid, (S)-3-(1-(tert-Butoxycarbonyl)-1H-imidazol-4-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid, PubChem12026, AC1ODZ1Y, SureCN3008885, CTK3J1699, MolPort-002-507-582, ANW-58552, AKOS015892674, AKOS015924152, AK-80245, FT-0081976, FT-0601960, ST51052629, M03293, A814986, (2S)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-3-[1-[(2-methylpropan-2-yl)oxy-oxomethyl]-4-imidazolyl]propanoic acid
IUPAC Name
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[1-[(2-methylpropan-2-yl)oxycarbonyl]imidazol-4-yl]propanoic acid
InChI Key
IXHPIPUIOSSAIS-NSHDSACASA-N
Density
1.22g/cm³
Exact Mass
355.17400
H-Bond Acceptor
7
H-Bond Donor
2

Upstream Synthesis Route 1

  • 24424-99-5
  • 71-00-1
  • 20866-46-0

Reference: [1]Patent: WO2019/118878,2019,A1 .Location in patent: Page/Page column 70

Upstream Synthesis Route 2

  • 24424-99-5
  • 645-35-2
  • 20866-46-0

Reference: [1]Journal of the Chemical Society, Dalton Transactions,1998,p. 1205 - 1212

Downstream Synthesis Route 1

  • 20866-46-0
  • 32926-43-5

Reference: [1] Chemistry of Natural Compounds, 1982, vol. 18, # 3, p. 322 - 327[2] Khimiya Prirodnykh Soedinenii, 1982, # 3, p. 349 - 354
[3] Chemistry of Natural Compounds, 1982, vol. 18, # 3, p. 322 - 327[4] Khimiya Prirodnykh Soedinenii, 1982, # 3, p. 349 - 354

Downstream Synthesis Route 2

  • 20866-46-0
  • 870-46-2
  • 17791-52-5

Reference: [1] Chemistry of Natural Compounds, 1982, vol. 18, # 3, p. 322 - 327[2] Khimiya Prirodnykh Soedinenii, 1982, # 3, p. 349 - 354

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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