Structure

Boc-Tyr-OH

CAS
3978-80-1
Catalog Number
ACM3978801
Category
Amino Acids
Molecular Weight
281.3

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Specification

Description
Building block for introduction of tyrosine amino-acid residues by Boc SPPS.
Synonyms
Boc-Tyr-OH, N-α-t.-Boc-L-tyrosine
InChI
1S/C14H19NO5/c1-14(2,3)20-13(19)15-11(12(17)18)8-9-4-6-10(16)7-5-9/h4-7,11,16H,8H2,1-3H3,(H,15,19)(H,17,18)
InChI Key
CNBUSIJNWNXLQQ-UHFFFAOYSA-N
Application
Peptide synthesis.
Assay
≥98% (TLC)
Form
powder
Functional Group
hydroxyl
MDL Number
MFCD00037179
Quality Level
200
Reaction Suitability
reaction type: Boc solid-phase peptide synthesis
Storage Temperature
2-30℃

Upstream Synthesis Route 1

  • 19391-35-6
  • 3978-80-1

Reference: [1]Synthesis,1980,vol. NO.11,p. 929 - 932
[2]Journal of the Chemical Society. Perkin transactions I,1977,p. 490 - 491

Upstream Synthesis Route 2

  • 1070-19-5
  • 3417-91-2
  • 3978-80-1
  • 70642-86-3

Reference: [1]Acta Chimica Academiae Scientiarum Hungaricae,1981,vol. 107,p. 7 - 9

Downstream Synthesis Route 1

  • 3978-80-1
  • 100-39-0
  • 2130-96-3

Reference: [1] Patent: US2005/283021, 2005, A1, . Location in patent: Page/Page column 6

Downstream Synthesis Route 2

  • 3978-80-1
  • 100-44-7
  • 2130-96-3

Reference: [1] Patent: US2005/283021, 2005, A1, . Location in patent: Page/Page column 6

Downstream Synthesis Route 3

  • 3978-80-1
  • 77-78-1
  • 53267-93-9

Reference: [1] Tetrahedron Letters, 2014, vol. 55, # 44, p. 6109 - 6112
[2] Patent: CN108003048, 2018, A, . Location in patent: Paragraph 0016
[3] Tetrahedron, 1993, vol. 49, # 17, p. 3521 - 3532

Downstream Synthesis Route 4

  • 74-96-4
  • 3978-80-1
  • 76757-91-0

Reference: [1]Journal of Organic Chemistry,1983,vol. 48,p. 4127 - 4129

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

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